FDA applicant

Accutech Medical Technologies, Inc.

Pleasanton, CA2 decisions2006–20090 recalls

FDA records 2 decisions for Accutech Medical Technologies, Inc. (Pleasanton, CA) from 2006 to 2009: 2 510(k) clearances. Most are in product codes FFS (Image, Illumination, Fiberoptic, For Endoscope) and GEX (Powered Laser Surgical Instrument). Its devices cite 10 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

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

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Accutech Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2007high 1 (2009) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Accutech Medical Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Accutech Medical Technologies, Inc.’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

Other applicant names beginning “Accutech”

FDA records each applicant name separately; these may or may not be the same firm.

Accutech, LLC 1

Accutech Medical Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Accutech”