10-Q · May 14, 2026
CapsoVision's Q1 2026 results show revenue of $2.79 million, marginally up from $2.78 million in the prior year, while gross margin decreased to 48% from 54% due to rising costs. Despite an EPS of -$0.15, slightly…
Earnings analysis · 10-Q
Filed August 13, 2026 · Our reading of the company's report
The latest report
CapsoVision delivered 10% year-over-year Q2 revenue growth to $3.643 million and reported a 13% increase in capsule volumes, but profitability deteriorated as operating expenses rose 46% and the operating loss expanded…
CapsoVision delivered 10% year-over-year Q2 revenue growth to $3.643 million and reported a 13% increase in capsule volumes, but profitability deteriorated as operating expenses rose 46% and the operating loss expanded to $7.580 million. Gross margin declined to 51% from 55%, while six-month operating cash use reached $14.469 million and management disclosed substantial doubt about the company's ability to continue as a going concern. Clinical and product milestones remain constructive, including completion of enrollment for the 801-patient CapsoCam Colon study and anticipated Q3 2026 AI clearance, but additional financing appears necessary and the new $100 million ATM creates significant dilution risk.
How much of each revenue dollar the business keeps.
One point per quarterly or annual filing. Both margins are shares of that report's revenue.
The business segments reported by the company.
Shares of the segments disclosed in this filing, largest first.
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Q2 revenue increased 10% year over year to $3.643 million from $3.315 million, driven primarily by a 13% increase in CapsoCam Plus capsules sold. International revenue increased 20% and represented 25% of total revenue versus 23% in the prior-year quarter.
Gross profit increased 3% to $1.871 million from $1.811 million, although gross margin declined to 51% from 55%. Management attributed the margin pressure to approximately 3% lower average selling prices, competitive pricing, and customs and tariff costs.
The second arm of the CapsoCam Colon pivotal study completed enrollment with 801 patients enrolled at up to 20 sites. Management expects to submit the related 510(k) application for the second-generation product in Q4 2026.
Management expects FDA clearance for the CapsoCam Plus AI feature by the end of Q3 2026 after submitting additional demographic analysis by the end of August 2026. The company had also commercialized the product in the EU by the filing date.
The company entered an at-the-market offering agreement on August 13, 2026 permitting sales of up to $100 million of common stock. Although there is no obligation to sell shares, the facility provides a potential source of liquidity.
The filing states that substantial doubt exists about the company's ability to continue as a going concern within one year. At June 30, 2026, cash was $9.077 million, while six-month operating cash usage was $14.469 million and management said existing cash would not fund operations for at least the next 12 months.
Operating expenses increased 46% year over year to $9.451 million, including a 57% increase in R&D expense to $5.309 million. The quarterly operating loss widened 63% to $7.580 million from $4.651 million, and the six-month accumulated deficit reached $170.2 million.
Cash and cash equivalents declined to $9.077 million from $10.112 million at December 31, 2025 despite $13.509 million of financing cash inflows. The company also reported a $1.717 million inventory cash outflow and $1.0 million of raw-material purchase commitments.
The new ATM program permits issuance of up to $100 million of common stock, creating a material potential dilution risk. Shares outstanding increased to 50.032 million at June 30, 2026 from 46.865 million at December 31, 2025 after the private placement and other equity issuances.
The company continues to face regulatory execution risk: the CapsoCam Colon 510(k) is planned for Q4 2026, while the CapsoCam Plus AI clearance is anticipated by the end of Q3 2026. The pancreatic-cancer UGI study had enrolled only 3 of up to 140 patients, and the company expects to resubmit its Breakthrough Device application after the study.
The filing highlights intensified tariff and supply-chain exposure. Six-month costs of revenue increased 16% to $3.235 million, including approximately $0.1 million of increased customs and tariff costs, while the company relies substantially on suppliers and contract manufacturers in Asia and had $2.3 million payable to Canon at June 30, 2026.
No numeric revenue or EPS guidance was provided. Management expects to submit the second-generation CapsoCam Colon 510(k) application in Q4 2026, expects FDA clearance for CapsoCam Plus AI by the end of Q3 2026 with U.S. commercialization shortly thereafter, and expects full commercialization of the capsule delivery device in Q4 2026.
CapsoVision's Q1 2026 results show revenue of $2.79 million, marginally up from $2.78 million in the prior year, while gross margin decreased to 48% from 54% due to rising costs. Despite an EPS of -$0.15, slightly…
CapsoVision reports continued commercial growth in its CapsoCam Plus franchise with CapsoCam Plus revenue of approximately $13.6 million in 2025 (up ~15% from $11.8 million in 2024) and >161,000 patients having used the…
CapsoVision reported Q3 2025 revenue of $3,538,000, up 19.3% year-over-year and ~6.7% sequentially, but profitability remains weak with an operating loss of $8,019,000 (operating margin -226.7%) and GAAP net loss of…
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