FDA applicant

Zap Lasers, LLC

Pleasant Hill, CA4 decisions2001–20090 recalls

FDA records 4 decisions for Zap Lasers, LLC (Pleasant Hill, CA) from 2001 to 2009: 4 510(k) clearances. All are in product code GEX (Powered Laser Surgical Instrument). Its devices cite 8 predicates, 4 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Zap Lasers, Inc.”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Zap Lasers, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2007high 1 (2008) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Zap Lasers, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Zap Lasers, LLC’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Zap Lasers, LLC

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?