Skip to content

Deuce Polypectomy Snare, Models 000995, 000996, 000997, 000998

by Conmed Endoscopic Technologies, Inc.

510(k) K091355

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK091355 Date22 Jul 2009ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
FDI
Models / Variants
Device Class
Class II
Regulation
21 CFR Part 876.4300
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 19 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Deuce Polypectomy Snare is a flexible snare device designed for endoscopic resection of polypoid lesions. It delivers electrosurgical current through a flexible endoscope to a stainless steel wire snare, facilitating precise removal of targeted tissue during endoscopic procedures.

This device is supplied as a sterile, single-use, disposable item intended for use in conjunction with an electrosurgical generator. It is classified under FDA regulation 876.4300 as a Class II medical device, with clearance through a 510(k) submission (K091355) and advisory review by the Gastroenterology and Urology committees. Models 000995, 000996, 000997, and 000998 are intended for use in gastroenterology and urology settings.

Other devices from Conmed Endoscopic Technologies, Inc.