FDA applicant

Endo Surgical Devices, Inc.

Hopkonton, MA2 decisions2002–20030 recalls

FDA records 2 decisions for Endo Surgical Devices, Inc. (Hopkonton, MA) from 2002 to 2003: 2 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and DWX (Stripper, Artery, Intraluminal). Its devices cite 1 predicate, 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, general and plastic surgery panel, where it files most

How often FDA has decided Endo Surgical Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Endo Surgical Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Endo”

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

Endo Lase, Inc. 24 Endo Technic Corp. 10 Endo-Therapeutics, Inc. 7 Endo GI Medical 2 Endo Surgical Concepts, Inc. 2 Endo Tools Therapeutics S.A. 2 Endo Twinn B.V. 2 Endo Optics, Inc. 2 Endo-Scientific, Inc. 2 Endo Vantage, LLC 1 Endo-Aid, Inc. 1 Endo Smart Cap Co. 1

Endo Surgical Devices, Inc.

Which product codes does it file in?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Endo”