Skip to content

Condor 3RXT7B

by Grainger International, Inc.

Condor 3RXT7B is a Class I device made by Grainger International, Inc., listed in FDA GUDID since 22 Dec 2025 (UDI-DI 10194484322141), 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 Number10194484322141 UDI-DI Date22 Dec 2025ListedStatusListed 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  • Withdrawn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
Condor
Generic name
Wrist orthosis
Model / reference
3RXT7B
Primary DI / UDI-DI
10194484322141
FDA product code
IMS
GMDN term
Wrist orthosis
Device class
Class I
Regulation number
890.3910
GUDID distribution status
In Commercial Distribution

Other devices from Grainger International, Inc.

See all devices from Grainger International, Inc. →

Properties

  • Contains latex
  • Premarket exempt
Other properties (13, all answered No)