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Fast-Fix 72202675

by Smith & Nephew, Inc.

Fast-Fix 72202675 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 29 Aug 2015 (UDI-DI 00885554023176), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885554023176 UDI-DI Date29 Aug 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Fast-Fix
Generic name
Suture knot pusher, single-use
Model / Ref / Catalog
72202675
Primary DI / UDI-DI
00885554023176
FDA product code
NBH
GMDN term
Suture knot pusher, single-use
Device class
Class I
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Suture knot pusher, single-use

Similar devices

Other devices filed under FDA product code NBH (ACCESSORIES,ARTHROSCOPIC).

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)