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7209391F

by Smith & Nephew, Inc.

7209391F is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 14 Jul 2016 (UDI-DI 00885556570029), 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 Number00885556570029 UDI-DI Date14 Jul 2016ListedStatusListed 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  • Withdrawn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

Generic name
Line-powered surgical power tool system motor
Model / Ref / Catalog
7209391F
Primary DI / UDI-DI
00885556570029
FDA product code
HAB
GMDN term
Line-powered surgical power tool system motor
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Line-powered surgical power tool system motor

Similar devices

Other devices filed under FDA product code HAB (SAW, POWERED, AND ACCESSORIES).

Other devices from Smith & Nephew, Inc.

See all devices from Smith & Nephew, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)