Skip to content

Non-Stick Bipolar Forceps

by Silverglide Surgical Technologies

510(k) K992931

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 NumberK992931 Date17 Nov 1999ClearedStatusActive

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  • Withdrawn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
GEI
Device Class
Class II
Regulation
21 CFR Part 878.4400
Advisory Committee
General, Plastic Surgery
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.

Non-Stick Bipolar Forceps are surgical instruments designed to address tissue adhesion and thermal damage during surgery. They feature micro-gauge tines that enable optimal tissue manipulation and are designed for precise operations.

These forceps are reusable and have a standard two-pin round connector that works with most standard foot-switching bipolar electrosurgical generators. They are authorized under FDA 510K clearance with product code GEI and model number K992931.

Questions

AI-generated answers, 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.

  • What is the purpose of the Non-Stick Bipolar Forceps?

    These forceps are designed to address tissue adhesion and thermal damage during surgery, featuring micro-gauge tines for optimal tissue manipulation and precise operations.

  • Are the Non-Stick Bipolar Forceps reusable or single-use?

    The forceps are reusable instruments designed for multiple surgical procedures, making them a cost-effective option for surgical facilities.

  • What type of connector do these forceps have?

    They feature a standard two-pin round connector that is compatible with most standard foot-switching bipolar electrosurgical generators.

  • What is the regulatory status of these forceps?

    The device is authorized under FDA 510K clearance with product code GEI and model number K992931, indicating it has been determined substantially equivalent to predicate devices.