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CellaVision (CEVI) investor relations material

CellaVision Q2 2026 earnings summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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Q2 2026 earnings summary17 Jul, 2026

Executive summary

  • Net sales reached SEK 200 million in Q2 2026, up 4.5% year-over-year, with 5.6% organic growth despite currency headwinds.

  • Americas achieved record sales, up 60% to SEK 105 million, driven by large instrument demand and automation trends.

  • EMEA stabilized after inventory adjustments, launched the Bone Marrow Aspirate (BMA) Application with initial sales and customer interest.

  • APAC faced a 59% sales decline due to tough China comparisons, but saw strong reagent growth in Japan and Australia.

  • CEO transition completed, incurring SEK 9 million in costs.

Financial highlights

  • Gross margin improved to 70% from 68% year-over-year, with gross profit at SEK 141 million.

  • EBITDA was SEK 55 million (27% margin), impacted by SEK 9 million CEO transition costs.

  • Operating expenses totaled SEK 100 million, up from SEK 79 million, mainly due to higher admin costs.

  • Operating cash flow was SEK 29 million; total cash flow was SEK -58 million, reflecting SEK 66 million in dividends.

  • Cash and cash equivalents stood at SEK 172 million at quarter-end.

Outlook and guidance

  • Strong order books in Americas and EMEA support a robust outlook for H2 2026.

  • BMA Application expected to contribute incremental growth as commercialization expands; FDA clearance targeted by year-end.

  • Continued investment in innovation and digital transformation to drive long-term value.

  • Financial ambition remains a CAGR of >15% and EBITDA margin >30% over the economic cycle.

  • R&D capitalization to increase in Q3 as projects mature, with gradual overall R&D cost growth.

Impact of China cost containment on APAC growth
Effect of R&D capitalization shift on margins
Drivers for sustained Americas instrument demand
Drivers of record Americas growth in Q2 2026?
Timeline for US Bone Marrow 510(k) clearance
FPM expansion into pathology and cytology
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