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LiteGait ALL LiteGait devices

by Mobility Research, Inc

Ref LiteGait

LiteGait ALL LiteGait devices is a gait rehabilitation system harness (EU MDR Class I; FDA Class I; FDA product code FSA, Lift, Patient, Non-Ac-Powered) made by Mobility Research, Inc, registered in EUDAMED on 3 Aug 2026 (Basic UDI-DI 0850040235LG6S) and listed in FDA GUDID since 13 Jul 2023 (UDI-DI 00850040235012), active as of 24 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0850040235LG6S Basic UDI-DI 00850040235012UDI-DIDate3 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00850040235012 UDI-DI Date13 Jul 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0850040235LG6S registered 3 Aug 2026 Active
  • FDA GUDID UDI-DI 00850040235012 listed 13 Jul 2023 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00850040235012
  2. Registered EUDAMED 0850040235LG6S

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
LiteGait
Generic name
Gait rehabilitation system harness
Model / Ref / Catalog
LiteGait EUDAMED
ALL LiteGait devices GUDID
Primary DI / UDI-DI
00850040235012
Basic UDI-DI
0850040235LG6S
FDA product code
FSA
EMDN code
Y050201 Standing support gait trainers
GMDN term
Gait rehabilitation system harness
Device class
Class I
Regulation number
880.5510
EU registration type
Standard device
EU market of registration
Denmark
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
LiteGait
GUDID
ALL LiteGait devices

Related devices

Category: Gait rehabilitation system harness

Similar devices in this category

Other devices filed under STANDING SUPPORT GAIT TRAINERS.

Other devices from Mobility Research, Inc

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (22, all answered No)