CellaVision AB (publ)
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About the company
CellaVision AB (publ), a company established in Lund, Sweden, in 1994, specializes in the development and distribution of digital analytical solutions for blood and body fluid samples. Their offerings cater to the healthcare services sector, with a significant global presence spanning Sweden, Europe, the Middle East, Africa, the Americas, and the Asia Pacific region. The company's product portfolio includes advanced hardware such as the CellaVision DM1200 and CellaVision DM9600, which are designed to automatically capture digital images from blood smears and various body fluid preparations, alongside the CellaVision DC-1 analyzer.
- CEO
- Steve Ferguson
- IPO
- 2013
- Employees
- 251
- HQ
- Lund, SN, SE
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- Market Cap
- $333.92M
- P/E
- 29.98
- Fwd P/E
- 2.36
- PEG
- -2.04
- P/S
- 5.23
- P/B
- 4.37
- EV/EBITDA
- 18.00
- Div Yield
- 1.70%
- Gross Margin
- 68.71%
- Op Margin
- 22.23%
- Net Margin
- 17.46%
- ROE
- 14.59%
- ROIC
- 12.66%
Latest fiscal year · YoY change
- Revenue
- $758.97M+4.9%
- Gross Profit
- $519.88M+6.7%
- Op Income
- $202.07M
- Net Income
- $153.08M+8.8%
- EPS
- $6.42+8.8%
- OCF Growth
- +1.1%
- FCF Growth
- -5.3%
- 52W High
- $19.28
- 52W Low
- $13.49
- 50D MA
- $13.92
- 200D MA
- $15.35
- Beta
- 0.97
- RSI (14)
- 79
- Avg Volume
- 28
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
CellaVision posted a solid Q2 rebound with record Americas sales, stable EMEA, and continued progress on bone marrow and FPM innovation.· July 17, 2026
- Net sales rose to SEK 200 million, up 4.5% year over year; organic growth was 5.6% with a 1.1% FX headwind.
- EBITDA was SEK 55 million with a 27% margin, including SEK 9 million of CEO transition costs.
- Americas hit an all-time high at SEK 105 million, driven by large instruments, tender wins, and refresh cycles.
- EMEA was stable but still affected by the concluded distributor inventory adjustment; management said Q3 orders are returning to normal.
- APAC remained challenging in China, but reagent growth in Japan and Australia was strong and recurring.
- Bone Marrow Aspirate launched in EMEA with encouraging initial sales; U.S. 510(k) clearance is still targeted before year-end.
Net sales were SEK 200 million in Q2 2026, up 4.5% year over year, or 5.6% organic growth, with a 1.1% currency headwind. EBITDA was SEK 55 million, implying a 27% EBITDA margin; management said EBITDA would have increased versus last year excluding SEK 9 million of CEO transition costs. Gross margin was 70%. Operating cash flow was SEK 29 million, working capital increased by SEK 32 million, total cash flow was minus SEK 58 million including a SEK 66 million dividend, and cash and cash equivalents ended at SEK 172 million. By region, Americas sales were SEK 105 million versus SEK 66 million last year, EMEA was SEK 75 million, and APAC was SEK 19 million. Management did not provide full-year financial guidance, but said Q3 order books look strong in EMEA and Americas, expected capitalized R&D to rise from Q3, and reiterated the goal of U.S. bone marrow 510(k) clearance before year-end.
Steve Ferguson framed Q2 as a recovery from a slower start to the year and emphasized commercial execution alongside innovation. He repeatedly pointed to stronger partnership work, especially with the main distributor/Sysmex relationship, and said there is still room to expand into smaller labs and other segments where CellaVision is less present. He also highlighted Bone Marrow Aspirate and FPM as important steps beyond core hematology, describing the pipeline as a foundation for future growth and adjacent-market expansion.
Monica Jonsson said the quarter delivered SEK 200 million in sales, 70% gross margin, SEK 100 million in operating expenses, and SEK 55 million EBITDA. She broke out the margin pressure from SEK 9 million of CEO transition costs, higher amortization on bone marrow and software development, and lower capitalization of R&D at SEK 15 million versus SEK 20 million last year, which made R&D expense look higher in the quarter. Cash generation remained solid at SEK 29 million operating cash flow, though working capital rose SEK 32 million due to receivables and inventory build for summer, and the balance sheet stayed strong with SEK 172 million in cash. She also said capitalization should increase from Q3 as projects mature, and that administration costs included some consultant costs, salary increases from April 1, and IT investments.
Analysts focused on whether the strong Americas print reflected channel stuffing or a genuine demand step-up; management said there was no evidence of stuffing, described the pattern as normal inventory consumption and refresh/tender activity, and said visibility into partner inventories is improving. On EMEA, management said the distributor destocking was now complete and Q3 orders are returning to normal. Questions on Bone Marrow Aspirate were answered with a reiteration that U.S. clearance is still expected by year-end and that management still sees the product contributing about 1% to 2% growth by year-end. Analysts also pressed on APAC reagent growth and R&D expense trends; management said Japan and Australia are driving recurring reagent revenue, and that R&D spending and capitalization should both rise gradually as projects mature.
The call showed clear demand momentum in the Americas, with record sales in a high-value instrument category and management saying the quarter was driven by real tender wins and refresh cycles rather than one-off stocking. Bone Marrow Aspirate has launched with encouraging early customer interest, and FPM is advancing as a platform for future innovation, giving the company multiple growth vectors beyond the core franchise.
EMEA still carried the hangover from distributor inventory adjustments, and APAC remains weak in China even as other markets improve. Profitability also absorbed SEK 9 million of CEO transition costs, and management noted higher admin spend, lower R&D capitalization in Q2, and ongoing uncertainty around transition-related expenses. Bone marrow in the U.S. is still awaiting 510(k) clearance, so the commercial upside remains dependent on regulatory timing and long customer evaluation cycles.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 58.9%
- Shares Outstanding
- 23.85M
- Float Shares
- 14.05M
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Generate CLVSF report →CellaVision AB (publ) (CLVSF) Q2 2026 Earnings Call Transcript
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CellaVision AB (publ) (CLVSF) Q3 2025 Earnings Call Transcript
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