PLSENasdaqSurgical & Medical Instruments & ApparatusUS GAAP · USD

Pulse Biosciences, Inc

Pulse Biosciences is a U.S.-based medical technology company focused on developing and commercializing nonthermal pulsed field ablation systems. Its platform includes the nPulse system and related disposable electrodes for use in surgical and minimally invasive procedures, with applications in cardiac arrhythmia treatment and soft-tissue ablation.

Revenue0.4m USD
Operating profit (EBIT)-76.9m USD
−36.8 %y/y
EBIT margin-21,982.6%
Net income-72.8m USD
−35.8 %y/y
Free cash flow-54.4m USD
−49.3 %y/y

Fiscal year 2025 · change from previous year

Development 2020–2025

-80-60-40-20020m USD2020: 0.00 m USD2020: EBIT -50 m USD20202021: 1.4 m USD2021: EBIT -63 m USD20212022: 0.70 m USD2022: EBIT -58 m USD20222023: 0.00 m USD2023: EBIT -44 m USD20232024: 0.00 m USD2024: EBIT -56 m USD20242025: 0.35 m USD2025: EBIT -77 m USD20250.35-77
RevenueOperating profit (EBIT)

Business

Share of revenue
Pulsed field ablation systems45 %

Console-based systems used to deliver nonthermal energy for tissue ablation.

Disposable electrode products35 %

Single-use electrodes and related consumables used with the company's platform.

Clinical-stage product development20 %

Development programs for atrial fibrillation, tumors, and nodules.

Customers

The company sells into clinical end markets that use ablation technologies, especially electrophysiology, cardiac surgery, and minimally invasive surgery. Its buyers are hospitals, physicians, and procedural specialists that need devices for treating atrial fibrillation and other soft-tissue conditions. The business also depends on clinical investigators and trial sites that support product development and regulatory progress.

Electrophysiology practices

Buy ablation systems for atrial fibrillation procedures and value differentiated energy delivery.

Hospitals and surgical centers

Use the platform in procedural settings for cardiac and soft-tissue ablation.

Cardiac surgeons

Adopt the system for surgical ablation workflows where direct support and training matter.

Clinical research sites

Support trials and early clinical use of the company's product candidates.

Strategy

The company is focused on advancing its nonthermal pulsed field ablation platform into marketable products for atrial fibrillation, tumors, and nodules. A key priority is building clinical evidence and product performance that can compete against established ablation technologies while expanding sales, marketing, and support capabilities. It also relies on third-party relationships and direct sales execution to translate development progress into adoption.

Develop marketable products for AF and soft-tissue ablationMedium term

Commercial success depends on turning the platform into approved, usable products.

Differentiate against micro-PFA and thermal ablation competitorsShort term

The market is crowded and technology cycles are fast, so performance advantages matter.

Expand sales, marketing, and clinical supportShort term

Adoption in procedural medicine depends on training, relationships, and hands-on support.

Geography

Pulse Biosciences is headquartered in the United States, with corporate offices in Miami, Florida. The reports indicate a domestic and international commercialization ambition, but no country-level revenue disclosure was provided in the excerpts. Geography matters because the company must build sales, clinical, regulatory, and support capabilities across markets where ablation adoption and reimbursement can differ.

Risks

The company faces substantial product-development and commercialization risk because its platform must prove safety, efficacy, and clinical utility against larger competitors with more resources. It also faces execution risk in sales, manufacturing, and distribution, along with litigation, product liability, and insurance coverage constraints that are common in medical devices. Accounting risk is elevated by goodwill and intangible asset impairment exposure, stock-based estimates, and judgment-heavy disclosures tied to a development-stage business.

Sorted by severity
Product development failureCritical

The business depends on creating marketable products for AF and other indications.

Exposure: nPulse System and future product candidates

Competitive displacementHigh

Established ablation companies have greater resources and faster product cycles.

Exposure: AF ablation and micro-PFA markets

Product liability and clinical trial claimsHigh

Medical devices can cause adverse events and trigger litigation or insurance losses.

Exposure: Manufactured products and trial-related events

Commercialization and channel executionMedium

Sales depend on trained reps, distributors, and direct procedural support.

Exposure: Domestic and international sales force

Accounting

Judgemental items
Goodwill and intangible asset impairment

The company has goodwill and intangibles from prior acquisitions that require periodic testing.

Impact: Could create non-cash charges and reduce reported asset values

Contingencies and product liability reserves

Claims from products or clinical trials require judgment on probability and magnitude.

Impact: Affects liabilities, expenses, and perceived financial strength

Section 382 net operating loss limitations

Ownership changes can restrict the use of pre-change tax losses.

Impact: May limit future tax benefit recognition

Publicly listed companies with a comparable business focus.

Last updated: 29/04/2026