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L'timate Knee Wrap Universal 50007260

by Bird & Cronin, LLC

L'timate Knee Wrap Universal 50007260 is a Class I device made by Bird & Cronin, LLC, listed in FDA GUDID since 20 Aug 2022 (UDI-DI 00610570114771), 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 Number00610570114771 UDI-DI Date20 Aug 2022ListedStatusListed 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  • Withdrawn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
L'timate Knee Wrap Universal
Generic name
Knee sling
Model / reference
50007260
Primary DI / UDI-DI
00610570114771
FDA product code
ITQ
GMDN term
Knee sling
Device class
Class I
Regulation number
890.3475
GUDID distribution status
In Commercial Distribution

Related devices

Category: Knee sling

Other devices from Bird & Cronin, LLC

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Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)