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Cytek Biosciences (CTKB) 2026年第三季度业绩电话会:毛利率达到59%

2026年11月6日 08:10
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Cytek Biosciences公布2026年第三季度营收为5320万美元,同比增长2%,主要受美国市场12%的增长带动。GAAP毛利率从上年同期的53%升至59%,得益于产品和服务毛利率提升、材料成本下降、关税降低以及制造转移至新加坡。Aurora和Aurora EVO合计装机量同比增长23%,累计装机量达4073台。服务营收同比增长13%,服务与试剂合计营收占过去12个月总营收的36%。Cytek将2026年全年营收指引区间收窄至2.08亿至2.11亿美元,中值保持不变,预计调整后EBITDA在盈亏平衡线附近。亚太地区营收同比下降25%,主要因宏观经济因素承压。

该摘要由AI生成

核心要点

  • Cytek Biosciences公布2026年第三季度营收为5320万美元,同比增长2%,主要受美国市场12%的增长带动。
  • GAAP毛利率从上年同期的53%升至59%,主要得益于产品和服务毛利率提升、材料成本下降、关税降低,以及生产制造从西雅图转移至新加坡。
  • Aurora和Aurora EVO合计装机量同比增长23%,其中Aurora EVO装机量接近翻倍。公司该季度新增140台仪器,累计装机量达4073台。
  • 服务营收同比增长13%。服务与试剂合计营收达1910万美元,占过去12个月总营收的36%,高于上年同期的33%。
  • Cytek将2026年全年营收指引区间收窄至2.08亿至2.11亿美元,同时维持中值不变。管理层仍预计调整后EBITDA将在盈亏平衡线附近。
  • 亚太地区营收依然承压,虽环比增长5%,但同比下降25%。在去年同期基数较高的背景下,生物制药、分销商及CRO相关营收同比下降约17%。

核心财务业绩

指标2026年第三季度变动 / 详情
营收5320万美元同比增长2%
产品营收3720万美元同比下降3%
服务营收1600万美元同比增长13%
GAAP毛利润3120万美元GAAP毛利率为59%
GAAP毛利率59%2025年第三季度为53%;提升近600个基点
产品毛利率61%上年同期为53%;提升770个基点
服务毛利率53%上年同期为51%
运营费用3960万美元同比增长8%
营业亏损840万美元较上年同期920万美元的亏损有所收窄
GAAP净亏损610万美元上年同期为亏损550万美元
调整后EBITDA70万美元低于上年同期的250万美元
现金、受限现金及有价证券2.56亿美元截至2026年6月30日为2.62亿美元

业务与运营表现

美国市场实现营收3040万美元,同比增长12%,得益于高端仪器需求、学术和政府客户以及服务业务的增长。欧洲、中东和非洲地区(EMEA)在连续两个季度下滑后,营收增长1%至1250万美元。包括中国在内的亚太地区实现营收830万美元,虽环比增长5%,但同比下降25%。

全球各地区学术和政府客户营收同比增长38%至2450万美元。在美国市场,来自该终端市场的仪器营收增长超过60%。相比之下,生物制药、分销商及CRO相关营收下降约17%至2870万美元,部分反映出亚太和中国市场的疲软以及去年同期的高基数效应。

高端平台仍是主要的产品驱动力。Aurora、Aurora EVO和Borealis系列营收增长超过30%,而高端全光谱分析仪器营收增长11%。Aurora和Aurora EVO合计装机量增长23%,其需求受到多色大Panel检测性能、高通量和自动化能力的有力支撑。

Cytek在本季度将Borealis的抢先体验计划规模扩大了一倍。管理层计划在第四季度进一步扩大该计划,并力争在2027财年进行更广泛的商业化推广,包括整合成像功能。

截至季度末,Cytek Cloud用户量接近3万名,较2026年初增长逾20%。管理层表示,该平台主要作为一个连接仪器、试剂、Panel设计和数据分析的生态系统,而非独立的利润来源。

管理层业绩指引

在假设当前汇率保持不变的前提下,Cytek将2026年全年营收指引区间收窄至2.08亿至2.11亿美元,中值保持不变。

管理层预计第四季度营收将显著高于第三季度,这符合常规季节性规律、年终客户采购周期以及服务业务的持续增长。预计服务营收将保持与近几个季度类似的增速,剩余部分由产品营收补齐。

公司仍预计全年调整后EBITDA将在盈亏平衡线附近。管理层表示,第四季度盈利能力将受益于更高的季节性营收以及诉讼费用环比减少300万至400万美元。

对于2027年,Cytek未提供具体数字指引。管理层表示,在高端产品、Borealis上市以及对中低端仪器和试剂投资的支撑下,公司预计增速将跑赢市场,并进一步提升盈利能力。

风险与关注重点

  • 亚太和中国市场同比依然疲软,管理层将其归因于这些市场的宏观经济因素。
  • 产品营收下滑,因高端分析仪的强劲表现被成像及中低端仪器销售额的下滑所抵消。
  • 第四季度指引在一定程度上取决于常规年终采购模式及季节性营收增长。
  • 一般及行政开支增长14%至1840万美元,其中包括与8月庭审相关的专利诉讼费用增加的300万美元。
  • 在这起专利案件中,陪审团在四项主张权利要求中的三项上支持了Cytek。在第四项上,陪审团裁定不存在字面侵权,但依据等同原则裁定侵权。Cytek已提交审后动议,并表示该裁决无需更改产品或运营,亦不影响其销售和发货产品的能力。
  • 公司新事业部架构的推行已推迟至2027年初,以降低年中重组带来的执行风险。

分析师问答要点

管理层表示,宏观市场环境较2025年初有所改善,并将当前状况定性为总体向好。

尽管第三季度有所下滑,但生物制药营收年初至今仍增长3%。管理层对美国市场保持乐观,理由是年终预算充足以及Aurora EVO具备的高通量和自动化特性。管理层还指出,分销商占比较高的亚太地区销售额计入生物制药、CRO及分销商类别中,放大了该地区疲软带来的影响。

在供应方面,管理层表示大多数订单在同一季度内完成预订和发货。Borealis和自动化升级版Aurora EVO系统的产量正在增加,公司并不认为供应限制是一个重大问题。

业绩电话会完整纪要


完整财报电话会议逐字稿

管理层陈述

Operator

Hello, and thank you for standing by. My name is Lacy, and I will be your conference operator today. At this time, I would like to welcome everyone to the Cytek Biosciences Third Quarter 2026 Earnings Conference Call. [Operator Instructions] Thank you. I would now like to turn the call over to Mark Meehan, Head of Investor Relations. Please go ahead.

Mark Meehan

Thank you, operator. Joining me today from Cytek are Wenbin Young, CEO; and Bill McCombe, CFO. Earlier today, Cytek Biosciences released financial results for the third quarter ended September 30, 2026. If you haven't received this news release or if you'd like to be added to the company's distribution list, please send an e-mail to investors@cytekbio.com. A copy of the news release is also available on the Investor Relations section of Cytek's website at investors.cytekbio.com. Please note that we will be referencing a slide presentation during the call today that has been posted to the Investors section of our corporate website.

As a reminder, on Slide 2, we will make statements during this call that are forward-looking statements within the meaning of the federal securities laws, including statements regarding Cytek's business plans, strategies, opportunities and financial projections. These statements are based on the company's current expectations and inherently involve significant risks and uncertainties that could cause actual results or events to materially differ from those anticipated in these statements. Additional information regarding these risks and uncertainties appears in our slide presentation in the section entitled Forward-Looking Statements in the press release Cytek issued today and in Cytek's filings with the SEC.

This call will also include a discussion of certain financial measures that are not calculated in accordance with generally accepted accounting principles. Additional information regarding our use of non-GAAP financial measures, including reconciliations to the most directly comparable GAAP financial measures may be found in our slide presentation and in today's press release. While the company believes these non-GAAP financial measures provide useful information for investors, the presentation of this information is not intended to be considered in isolation or as a substitute for the financial information presented in accordance with GAAP.

This call will also provide a brief update about our active patent litigation. For more complete information about this case as well as countersuits that we have instituted, please refer to our previous press release as well as our SEC filings, including our Form 10-Q to be filed today. Except as required by law, Cytek disclaims any duty to update forward-looking statements, whether because of new information, future events or changes in its expectations. This conference call contains time-sensitive information and is accurate only as of the live broadcast, November 4, 2026.

With that, I will turn the call over to Wenbin.

Wenbin Jiang

Thanks, Mark. Welcome, everyone, and thank you for your interest in Cytek. On today's call, I will start with a discussion on our performance in the third quarter and review some business highlights before turning the call over to Bill for a detailed look at our financial results and our full year outlook. Turning to Slides 3 and 4. We delivered another solid result in the third quarter with revenue of $53.2 million, an increase of 2% year-over-year. Our third quarter was highlighted by growth in the U.S. driven by continued strong demand for our high-end full spectrum profiling instruments led by Aurora EVO, the double-digit growth in our service business and by our robust gross margin performance.

Growth in the third quarter was led by the U.S., where revenue grew 12% year-over-year to $30.4 million, continued strong momentum from the first half, driven by instrument sales to academic and government customers and continued service growth. In EMEA, third quarter revenue was $12.5 million, up 1% year-over-year, a positive sign after a challenging first half that reflected improving instrument sales to academic and government customers. Total APAC revenue, including China was $8.3 million, up 5% sequentially versus Q2, while being down 25% compared to a strong Q3 last year.

Turning to Slide 5. The third quarter was highlighted by success at the high end, where our technology leadership continues to shine. Customers are choosing Aurora EVO as it lets them run large panels and get consistent reproducible data at higher throughput. The automation configurations we introduced last quarter further increased the value to customers with the API for automated handling system fitting well into the high-volume workflows of biopharma and CRO customers. Combined Aurora and Aurora EVO placements grew 23% year-over-year with EVO placements nearly doubling year-over-year, reflecting robust demand for our next-generation platform. As a result of strong placements, high-end full spectrum profiling instrument revenue grew 11%. Across the broader business, we added a total of 140 instruments in the quarter, bringing our total installed base to 4,073 units.

Borealis, our newest platform, which we introduced last quarter, is receiving strong interest from customers in both the academic and biopharma markets, and we doubled the size of our early access program during Q3. As a reminder, Borealis is a laser full spectrum profiling cytometer with 60 color performance already demonstrated and a clear path to go higher as new dyes and panels are developed. It will also include integrated imaging capabilities when we get to full commercial launch. Paired with our new proprietary cFluor reagents, Borealis enables 60 color panels in a single tube while also supporting nanoparticle analysis and higher sampling rates. Early access program customers are excited about how these capabilities can enhance insight and accelerate discovery in their labs. We will continue to expand the early access program in the fourth quarter with a broader commercial launch planned for fiscal year 2027.

Turning to Slide 6. During the third quarter, we launched a new Cytek Cloud analysis tool, the industry's first end-to-end platform that integrates the entire flow cytometry workflow from panel design to data analysis into one system. This will allow researchers to have a seamless experience from experiment planning through data analysis, reducing the need to move between systems or recreate workflows. Cloud analysis is available in the U.S. through Cytek Cloud Premium, a new subscription tier that adds cloud-based data analysis and online data storage. The launch is an important milestone towards our vision of Cytek Cloud as a comprehensive digital ecosystem that supports both cytometry workflows from beginning to end.

As of the end of the third quarter, the total Cytek Cloud user base is approaching 30,000, up more than 20% since the start of the year. Our recurring revenue base continued to grow in the third quarter. Combined service and reagent revenue was $19.1 million in Q3 2026 and represented 36% of Cytek's last 12 months revenue, up from 33% for the 12 months ended September 30, 2025. We expect recurring revenue to represent an increasing percentage of total revenue over time. During the quarter, we also had important developments in our patent litigation case. As we announced on August 21, a jury in the U.S. District Court for the District of Delaware found in our favor on 3 of the 4 asserted claims in both infringement and invalidity for each of those 3 claims. On the fourth claim, the jury found no legal infringement, but did find infringement under the adoption of equivalents. We do not believe that the applicable legal criteria for infringement and the adoption of equivalents have been met.

We filed posttrial motions asking the court to overturn the verdict on this and other grounds, and we intend to pursue all available legal remedies. The jury verdict does not require any change to our product offering or operations and our ability to sell and ship products is not affected. Notably, the patent is a U.S. patent and only applies to sales of instruments made in or imported into the United States.

Finally, I wanted to share an update on the new business unit structure we introduced earlier this year. After careful review, we have decided to postpone the implementation of these business units until the start of 2027. We judged the near-term risk of moving to our new organization structure midyear to be too significant. We remain confident that the new structure is the best way to support our long-term growth, but we recognize the critical need to deliver throughout the remainder of 2026. We are continuing to focus resources and build out our teams to grow our clinical and solution-focused instruments and reagents.

Stepping back, we were pleased with the overall performance of our business. The third quarter was highlighted by continued success of our high-end Aurora EVO and Polaris analyzers by the double-digit growth in our service business and as Bill will detail shortly, the strong execution from our operations team, which resulted in our best third quarter gross margins since 2023. With top line performance in line with our prior expectations, we are reiterating the midpoint of our full year 2026 revenue guidance. And with that, I will now turn the call over to Bill for additional details on our Q3 financials and our full year outlook.

William McCombe

Thanks, Wenbin. Turning to Slide 7. Third quarter revenue came in at $53.2 million, an increase of 2% compared to Q3 2025. The highlight for the quarter was the strong customer demand for our high-end analyzers with revenue growth of over 30% for the Aurora, Aurora EVO and Borealis category. This was the major factor driving U.S. total revenue growth of 12% and instrument growth of 9%. EMEA revenue returned to modest total revenue growth of 1% year-on-year and instrument growth of 3% after 2 quarters of declines. APAC, including China, grew 5% sequentially compared to Q2, but was down 25% compared to a strong Q3 '25. We saw particular strength in revenue from academic and government customers, which was up 38% year-over-year to $24.5 million, with strength across all regions. In the U.S., the largest region for the academic and government end market, instrument revenue grew more than 60%.

Biopharma distributor and CRO revenue declined approximately 17% year-over-year to $28.7 million against a strong Q3 last year. Product revenue, which is comprised of instruments and reagents was $37.2 million, a decrease of 3% year-over-year as strength in our high-end instruments was offset by declines in imaging and mid- to low-end instruments. Service revenue grew 13% year-over-year, driven by growth in our installed base and continued active utilization of our systems.

Turning to Slide 8. Turning to gross margin. As Wenbin mentioned, we had an outstanding result with GAAP gross profit of $31.2 million in Q3, representing a gross margin of 59% compared to 53% in Q3 2025, an increase of nearly 600 basis points as we benefited from both higher product gross margin and higher service gross margin. Product gross margin increased 770 basis points to 61% compared to 53% in Q3 last year. The increase was primarily due to lower overhead costs resulting from the completion of the transfer of manufacturing capacity from Seattle to Singapore and also lower material costs and lower tariffs. Service gross margin was 53%, up from 51% in Q3 2025, reflecting service revenue growth of 13%, which outpaced the 8% increase in service cost of sales.

We are now realizing the full benefit of the transfer of manufacturing from our Seattle site to our Singapore facility earlier this year. This move is part of our region-for-region manufacturing strategy, which gives us lower cost manufacturing capacity, greater supply flexibility and helps mitigate tariff-related cost pressures. Total operating expenses were $39.6 million in Q3, up 8% versus Q3 2025. Research and development expenses were $9.4 million, up 4%, while sales and marketing expenses were $11.9 million, up 2%. General and administrative expenses were $18.4 million, up $2.2 million or 14% compared to Q3 2025. This was due to a $3 million increase in legal expenses associated with our patent litigation and specifically the trial, which occurred in August. With the most expensive trial phase of this case behind us, we would expect our legal expenses to decline by $3 million to $4 million in the fourth quarter compared to Q3.

The loss from operations was $8.4 million in the third quarter compared to a $9.2 million loss in the year ago quarter. GAAP net loss was $6.1 million compared to a $5.5 million loss in the third quarter of 2025. The increase in GAAP net loss was due to a $1.5 million lower tax benefit, offset by a $0.8 million improvement in loss from operations. Adjusted EBITDA, which excludes stock-based compensation and foreign exchange gains and losses was $0.7 million in Q3 2026 compared to $2.5 million in Q3 2025. The decline was primarily due to lower investment income and higher operating expenses. We anticipate adjusted EBITDA to improve meaningfully in the fourth quarter as revenue increases with our normal seasonal pattern. Cash, cash equivalents, restricted cash and marketable securities totaled $256 million as of September 30, 2026, compared to $262 million as of June 30, 2026. Our strong balance sheet continues to provide the financial flexibility to invest in our global growth priorities.

Turning to Slide 9. We are maintaining the midpoint of our full year 2026 revenue guidance while narrowing the range to $208 million to $211 million. This assumes no change from current currency exchange rates. This reflects year-to-date results and the growth outlook across our markets. In the fourth quarter, we expect revenue to be meaningfully higher than in the third quarter, consistent with our normal seasonality, driven by typical customer year-end purchasing patterns and continued growth in our service business. For the full year 2026, we continue to expect adjusted EBITDA to be around breakeven, reflecting an anticipated strong fourth quarter results driven by the seasonal increase in revenue as well as a meaningful decrease in litigation spending. With that, I will turn it back over to Wenbin.

Wenbin Jiang

Thanks, Bill. I want to close by thanking the entire Cytek team for their continued dedication and execution on behalf of our stakeholders. Our third quarter was a solid one, and we expect a strong finish to the year. The results reflect the strength of our technology leadership in the flow cytometry industry. Looking ahead, we feel well positioned heading into next year. We continue to gain share as our new product portfolio strengthens our technology leadership position in biopharma and academic research markets. We also anticipate improving performance with clinical customers, driven by our new organizational structure and the benefits of our SMS collaboration in Europe. Finally, we expect to deliver improving profitability as we continue to drive leverage on increased volume and anticipate reduced G&A spend on litigation expenses. Thanks to everyone for joining today's call. We will now open it up for questions.

Operator

[Operator Instructions] Your first question comes from the line of Mason Carrico with Stephens.

分析师问答

Harrison Parsons

This is Harrison on for Mason. Could you just start by walking us through the guidance range for 2026? Should we expect service revenue to continue to grow around the low double-digit clip in the fourth quarter and product revenue to make up the balance there?

William McCombe

Yes. Our service revenue has grown fairly consistently. So we expect that to continue. And at similar rates to recent quarters and the product revenue would be -- would make up the balance. That's right.

Harrison Parsons

And then looking ahead here at 2027, I think you previously pointed to the second half '26 growth rate is a fair jumping off point for next year. Does that framework still hold today? And how are you thinking about growth next year across the different?

Wenbin Jiang

I don't think we've commented specifically on giving guidance for growth in 2027. So I'm not going to comment on your framework there. What I will say is that we will continue to -- and we'll give more specific guidance when we announce Q4 revenue in late February, early March. But we would expect to outgrow the market in 2027. We are continuing to invest in our high-end product portfolio. We're going to, as you know, bring to market the Borealis analyzer with full imaging capability. That's slated for launch in 2027. We are investing substantial resources in growing our low to mid-range instruments and our reagent portfolio. So we'll maintain leadership in the high end, and we'll continue to invest in growing our business. And we would expect improving profitability. And I can't really give more specific guidance beyond that. But we would -- based on those investments and based on our performance so far, we would expect to outgrow the market and outgrow our peers.

Operator

Your next question comes from the line of Chad Wiatrowski with TD Cowen.

Chad Wiatrowski

I appreciate continued taking market share next year, plan to outgrow the market. Do you still feel like the markets may be flat? Or do you think we've returned to growth here across end markets?

William McCombe

I think the market growth has been better really going back to the fourth quarter of last year and the first 3 quarters of this year, we have certainly done better than the early part of 2025. The market has been better. Some of the headwinds that occurred back then have abated. So I think we feel that the market environment is generally positive.

Chad Wiatrowski

And then I guess on the Cytek Cloud user base, the growth is pretty impressive. Just wondering if internally, do you guys view that as maybe more of a moat to your instruments as these tools are used more broadly across workflows? Or is this something you think -- I know you started to maybe monetize it a little bit previously, but do you feel like there's a lot of juice to squeeze here and maybe that could be upside to service revenues?

Wenbin Jiang

The intention of Cytek Cloud is not to really squeeze any profit out of the platform by itself, right? And it is a tool to enable our users to leverage our full solutions, including our instrument reagents and panel design, data analysis altogether. So customers will stay with what we have.

Operator

Your final question comes from the line of David Westenberg with Piper Sandler.

Skye Gilbert

This is Skye on for Dave. Maybe first, can you just talk a bit more about biopharma? You've seen some growth in the past from large pharma and biotech customers. I know you called out the tough comp this quarter, but has the momentum slowed at all? And what does that mean for CROs and some of the smaller customers? And ultimately, how much of the demand now is reflecting ongoing fleet deployments versus individual instrument purchases?

William McCombe

Well, I would point out that year-to-date, biopharma is up 3%. And look, it's generally been lumpy. We did have some strong quarters towards the back end of last year. The other factor that influences our numbers as reporting -- as reported is that a disproportionate -- much higher share of overall sales in Asia Pac and China go through distributors, which we report in the biopharma, CRO and distributor category. So as I think we noted, the markets in APAC and China in the third quarter were quite a bit weaker, but primarily due to macroeconomic factors in those markets. So that has sort of dampened the growth of what we report as the biopharma CRO distributor category. So I think it's important to bear that in mind.

But we think the biopharma sector, particularly in the U.S., that they have money available for a year-end budget flush. We think that the Aurora EVO because of its high throughput and its automation capabilities is an excellent product for that market. So we remain generally quite positive on that market segment.

Skye Gilbert

And just lastly, in September, I think for a few of the instruments, you mentioned you were selling everything you can make and that orders were generally booked and shipped within the quarter. Where are you still supply constrained? Are there lead times or ordering patterns or other cancellations giving you better visibility in demand at this time?

Wenbin Jiang

Yes. Other than the small amounts, we generally book and ship -- we generally ship everything that we book within a quarter. When I -- when we made those comments at the end of -- on the Q2 call, we were talking about Borealis and the Aurora EVO with the enhanced automation capability. We're continuing to increase our production rate of those types of systems. So we expect them to be important contributors going forward and products that are seeing good, very good demand from customers. The supply constraints is not really a huge -- not a big issue for us.

Operator

There are no further questions at this time.

Mark Meehan

Okay. Thanks. We will go ahead and end the call there. Thank you, everyone, for joining, and please reach out to us if you have any follow-up questions. Bye.

Operator

Ladies and gentlemen, you may now disconnect.

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