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CeriBell (CBLL) Q2 FY26 earnings call: guidance and Q&A

Earnings call· Jun 2026 (Q2 FY26)· Health Care· Aug 10, 2026

Source: earnings call transcript

Executive summary

CeriBell Q2 FY26 — Accelerating Revenue Growth and Delirium Commercialization

CeriBell reported strong Q2 FY26 results with accelerating revenue growth and record gross margins, fueled by robust same-store performance and account expansion. The company secured FDA clearances for new algorithms and a next-gen hardware platform, while its Delirium Monitoring Solution received favorable NTAP and is slated for commercial launch this year. Management is focused on achieving cash flow break-even and leveraging its expanding product portfolio for sustained long-term growth.

Highlights

5
  • Total revenue of $28.1 million, growing 33% year-over-year, accelerating from 29% in Q1.

  • Record gross margin of 92% (89% excluding tariff refund) driven by supply chain optimization.

  • Active account base increased by 32 accounts to a total of 712 hospitals.

  • FDA 510K clearances for two new algorithms (artifact rejection and epileptiform abnormality detection) enhancing clinical utility.

  • Favorable New Technology Add-on Payment (NTAP) for Delirium Monitoring Solution, effective October 1, 2026, providing up to $2,171 in incremental reimbursement per patient.

Concerns

3
  • Total operating expenses increased 37% year-over-year to $45.9 million, outpacing revenue growth.

  • Net loss was $19.3 million, or $0.51 per share, compared to a loss of $13.6 million ($0.38 per share) in Q2 FY25.

  • Elevated G&A expenses included $3.9 million related to ongoing IP litigation.

Guidance & targets

CategoryTargetConfidence
Full-year 2026 Total Revenue
$114 million to $117 million
high materiality
High
Gross Margin
high 80% range
medium materiality
High
Delirium Monitoring Solution Commercial Launch
Commercially launched this year
high materiality
High
New Hardware Platform Launch
Target launch in 2027
high materiality
Medium
Artifact Rejection Algorithm Rollout
Rolling out in the third quarter
medium materiality
High
Epileptiform Abnormality Detection Algorithm Activation
Activate this algorithm by the end of the year
medium materiality
High

Product announcements

ProductTypeDetails
Artifact Rejection Algorithmlaunch
Epileptiform Abnormality Detection Algorithmlaunch
New Hardware Platform (Recorder with video/ECG, vital sign integration, continuous monitoring)launch
New Headband Designslaunch

Deals & partnerships

Credit Facility Lenders Refinancing of existing credit facility Up to $60 million committed capital, additional $25 million uncommitted Repayment extended into 2031

Structure includes a non-formular revolver plus term loan available to draw through year-end 2028. No plans to draw the committed but undrawn term loan in the near term.

Risks & headwinds

IP Litigation Expenses Q2 FY26

$3.9 million in Q2 FY26

Mitigation:Anticipate a reduction in lawsuit-related activities and associated expense in Q3 and Q4 2026.

Seasonality in ICU Census Q2 FY26

Typical seasonality in Q2, with warmer months tending to result in reduced ICU census.

Mitigation:Same-store growth performance exceeded expectations despite this, indicating strong underlying demand.

Operating Expense Growth Outpacing Revenue Q2 FY26

Total operating expenses increased 37% YoY to $45.9 million, while revenue grew 33% YoY.

Mitigation:Management's strategy is to thoughtfully deploy gross profits from expanding revenue back into the business for long-term growth, while maintaining adjusted EBITDA loss around $10 million and aiming for cash flow break-even with cash on hand.

What to watch in Q3 FY26

Delirium Commercial Launch

Q4 2026
Current Commercial pilot live in multiple sites, NTAP effective Oct 1, 2026.
Target Successful commercial launch, initial revenue contribution.

Why it matters

Delirium represents an estimated $1 billion U.S. market and is expected to be a significant revenue driver in 2027.

Our launch strategy is coming into focus. And we now have the confidence that we will launch Gilerion commercially this year.

Find out whether CBLL delivers this. Inve re-checks your case every morning.

Q&A highlights

What is the revenue impact of the recent FDA approvals for algorithms and the new hardware platform?

New algorithm clearances (artifact rejection, epileptiform abnormality) will not be charged extra but are expected to increase stickiness and utilization, especially with neurologist support. The new hardware platform, launching in 2027, is aimed at making EEG a new vital sign for delirium and future LVO, and is expected to be a direct revenue driver.

“This new hardware platform really has been aiming at making EEG a new vital sign in junction to delirium and the future LVO we're working on. So we see this as giving us access to additional patients or even additional market segments. So we do see this can be a revenue driver in 2027 directly.”

asked by Travis Steed · answered by Unknown Speaker

2 min read 6 chapters

Detailed narrative

Commercial Momentum and Account Growth

CeriBell achieved 33% year-over-year revenue growth in Q2 FY26, accelerating from 29% in Q1, driven by strong same-store performance and an increase of 32 active accounts, reaching a total of 712 hospitals. The account acquisition team is maturing, and a newly established strategic account management team is building a robust pipeline, expected to accelerate new account additions in 2026 compared to 2025.

Early commercial traction from neonate and pediatric product lines is also contributing to new account openings and increased utilization within existing customer accounts.

Gross Margin Expansion and Supply Chain Optimization

The company reported a record gross margin of 92% in Q2, which included a $1.6 million tariff refund. Excluding this refund, the gross margin was 89%, reflecting proactive supply chain optimization and manufacturing diversification, particularly the shift to Vietnam. This strong margin profile is expected to be maintained in the high 80% range throughout 2026, providing capital for reinvestment into growth initiatives and R&D.

Delirium Monitoring Solution Progress

CeriBell's Delirium Monitoring Solution, which received 510K clearance in December, secured a favorable New Technology Add-on Payment (NTAP) from CMS, effective October 1, 2026. This NTAP provides up to $2,171 in incremental reimbursement per qualified patient. The commercial pilot has yielded positive feedback, with users reporting improved clinical decision-making and increased utilization among existing Cerebell customers.

The commercial launch of the solution is planned for Q4 2026.

Advanced Algorithm Development

The company received FDA 510K clearances for two new algorithms targeting its core seizure market. The first significantly enhances the Clarity algorithm's ability to identify and reduce EEG artifact signals, simplifying interpretation for neurologists. The second clearance is for epileptiform abnormality detection, making Cerebell the first software FDA cleared for both seizure and epileptiform abnormality detection.

These algorithms are anticipated to roll out in Q3 and by year-end 2026, respectively.

Next-Generation Hardware Platform

CeriBell has received FDA 510K clearances for several products that form the foundation of its new hardware platform. This includes a recorder with video and ECG capability, vital sign integration, and continuous monitoring. Two new headband designs offer optionality for full montage and multi-day continuous monitoring.

This platform aims to support the vision of making EEG a new vital sign, with a target launch in 2027, expanding access to additional patient populations and market segments.

Financial Position and Capital Management

CeriBell ended Q2 with $129.3 million in cash, cash equivalents, and marketable securities. The company successfully refinanced its existing credit facility, securing access to up to $60 million in committed capital with an additional $25 million uncommitted, extending repayment to 2031 and expected to reduce interest expense from Q4. Management reiterated its commitment to achieving cash flow break-even with existing cash on hand.

Summary of the company's earnings call; see how call summaries are prepared. Not investment advice.