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CAPS Professional

by Vestibular Technologies, LLC

CAPS Professional (P31C) is a Class I device made by Vestibular Technologies, LLC, listed in FDA GUDID since 1 Dec 2019 (UDI-DI B702P31C0), 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 NumberB702P31C0 UDI-DI Date1 Dec 2019ListedStatusListed 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  • Withdrawn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
Caps
Generic name
Biomechanical function analysis/interactive rehabilitation system
Model / Ref / Catalog
Professional, P31C
Primary DI / UDI-DI
B702P31C0
FDA product code
KHX, FRI
GMDN term
Biomechanical function analysis/interactive rehabilitation system
Device class
Class I
Regulation number
890.1575, 880.2700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Stand-on floor scale, electronicPosturography system platformBiomechanical function analysis/interactive rehabilitation systemPosturography system

Similar devices

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

Other devices from Vestibular Technologies, LLC

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)