FDA applicant

Conmed Endoscopic Technologies, Inc.

Billerica, MA2 decisions2008–20090 recalls

FDA records 2 decisions for Conmed Endoscopic Technologies, Inc. (Billerica, MA) from 2008 to 2009: 2 510(k) clearances. Most are in product codes KNS (Unit, Electrosurgical, Endoscopic (With Or…) and FDI (Snare, Flexible). Its devices cite 5 predicates, 0 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 Conmed Endoscopic Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2009

2008high 1 (2008) · low 0 (2010)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Conmed Endoscopic Technologies, Inc. by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Conmed Endoscopic 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 “Conmed”

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

Conmed Corporation 84 Conmed Linvatec 21 Conmed Andover Medical, Inc. 8 Conmed Integrated Systems (Cmis) 5 Conmed Electrosurgery 1 Conmed Corporation, Largo 1 Conmed Integrated Systems, Canada, Ulc 1 Conmed Linvatec Biomaterials 1

Conmed Endoscopic Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Conmed”