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Vive Mobility MOB1113

by Vive Health LLC

Vive Mobility MOB1113 is a Class I device made by Vive Health LLC, listed in FDA GUDID since 5 Sep 2024 (UDI-DI 00810113578293), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810113578293 UDI-DI Date5 Sep 2024ListedStatusListed 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  • Withdrawn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
Vive Mobility
Generic name
Handgrip disability-assistive walker, non-powered, foldable
Model / reference
MOB1113
Primary DI / UDI-DI
00810113578293
FDA product code
ITJ
GMDN term
Handgrip disability-assistive walker, non-powered, foldable
Device class
Class I
Regulation number
890.3825
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ITJ (Walker, Mechanical).

Other devices from Vive Health LLC

See all devices from Vive Health LLC →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)