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Equipoise Eqpos

by Equidor Medtech LLP

Equipoise Eqpos is a Class I device made by Equidor Medtech LLP, listed in FDA GUDID since 19 Feb 2025 (UDI-DI 08908024776005), 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 Number08908024776005 UDI-DI Date19 Feb 2025ListedStatusListed 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  • Withdrawn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
Equipoise
Generic name
Posturography system
Model / reference
EQPOS
Primary DI / UDI-DI
08908024776005
FDA product code
KHX
GMDN term
Posturography system
Device class
Class I
Regulation number
890.1575
GUDID distribution status
In Commercial Distribution

Related devices

Category: Posturography system

Similar devices

Other devices filed under FDA product code KHX (Platform, Force-Measuring).

Properties

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