FDA applicant

Endonetics, Inc.

Los Gatos, CA1 decision2000–20004 recalls

FDA records 1 decision for Endonetics, Inc. (Los Gatos, CA) in 2000: 1 510(k) clearance. All are in product code FFT (Electrode, Ph, Stomach). 4 recalls are 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 Endonetics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Endonetics, Inc. since 2007.

Recalls per year

2in 2016

2007high 2 (2016) · low 0 (2008)2026

Class I Class II/III not classified

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

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Endonetics, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?