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MedX Lumbar

by Medx Holdings, Inc.

MedX Lumbar is a core-body mechanical weight exerciser (FDA Class II; FDA product code ISD, Exerciser, Measuring) made by Medx Holdings, Inc., listed in FDA GUDID since 5 Jul 2017 (UDI-DI 00851688007016), 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 Number00851688007016 UDI-DI Date5 Jul 2017ListedStatusListed 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  • Withdrawn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
MedX
Generic name
Core-body mechanical weight exerciser
Model / reference
Lumbar
Primary DI / UDI-DI
00851688007016
FDA product code
ISD
GMDN term
Core-body mechanical weight exerciser
Device class
Class II
Regulation number
890.5360
GUDID distribution status
In Commercial Distribution

Related devices

Category: Core-body mechanical weight exerciser

Similar devices

Other devices filed under FDA product code ISD (Exerciser, Measuring).

Other devices from Medx Holdings, Inc.

Properties

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