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Flint Rehab MGML

by Flint Rehabilitation Devices, LLC

Flint Rehab MGML is a Class I device made by Flint Rehabilitation Devices, LLC, listed in FDA GUDID since 11 Aug 2023 (UDI-DI G144MGML0), 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 NumberG144MGML0 UDI-DI Date11 Aug 2023ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Flint Rehab
Generic name
Perceptual-coordination assistive training device
Model / reference
MGML
Primary DI / UDI-DI
G144MGML0
FDA product code
ION
GMDN term
Perceptual-coordination assistive training device
Device class
Class I
Regulation number
890.5370
GUDID distribution status
In Commercial Distribution

Related devices

Category: Perceptual-coordination assistive training device

Other devices from Flint Rehabilitation Devices, LLC

See all devices from Flint Rehabilitation Devices, LLC →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)