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MediChoice GAIT723

by Owens & Minor Distribution, Inc.

MediChoice GAIT723 is a Class I device made by Owens & Minor Distribution, Inc., listed in FDA GUDID since 14 Oct 2020 (UDI-DI 20885632061643), 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 Number20885632061643 UDI-DI Date14 Oct 2020ListedStatusListed 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  • Withdrawn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
MediChoice
Generic name
Gait rehabilitation system harness
Model / reference
GAIT723
Primary DI / UDI-DI
20885632061643
FDA product code
IQB
GMDN term
Gait rehabilitation system harness
Device class
Class I
Regulation number
890.3920
GUDID distribution status
In Commercial Distribution

Related devices

Category: Gait rehabilitation system harness

Other devices from Owens & Minor Distribution, Inc.

See all devices from Owens & Minor Distribution, Inc. →

Properties

  • Contains latex
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)