FDA applicant

Endoscopic Technologies, Inc. D/B/A Estech

San Ramon, CA5 decisions2009–20125 recalls

FDA records 5 decisions for Endoscopic Technologies, Inc. D/B/A Estech (San Ramon, CA) from 2009 to 2012: 5 510(k) clearances. Most are in product codes OCL (Surgical Device, For Cutting, Coagulation…) and GEI (Electrosurgical, Cutting & Coagulation &…). Its devices cite 9 predicates, 0 of them its own earlier devices. 5 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, general and plastic surgery panel, where it files most

How often FDA has decided Endoscopic Technologies, Inc. D/B/A Estech’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2009high 2 (2009) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

4in 2019

2009high 4 (2019) · low 0 (2009)2026

Class I Class II/III not classified

FIG. 1 — Endoscopic Technologies, Inc. D/B/A Estech by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Endoscopic Technologies, Inc. D/B/A…’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 “Endoscopic”

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

Endoscopic Technologies, Inc. 8 Endoscopic Concepts, Inc. 4 Endoscopic Surgical Products, Inc. 2 Endoscopic Surgical Accessories, Inc. 1 Endoscopic Innovations, Inc. 1

Endoscopic Technologies, Inc. D/B/A Estech

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?

What has been recalled?

Other applicant names beginning “Endoscopic”