Skip to content

CurveCapture CC-FM-ADH

by Curveassure Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860016054912 UDI-DI Date6 Aug 2026ListedStatusListed 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  • Withdrawn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
CurveCapture
Generic Name
Biomechanical function analysis system, motion-tracking
Model / Reference
CC-FM-ADH
Primary DI / UDI-DI
00860016054912
FDA Product Code
QKC
GMDN Term
Biomechanical function analysis system, motion-tracking
Device Class
Class II
Regulation Number
890.5360
GUDID distribution status
In Commercial Distribution

Other devices from Curveassure Inc.

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No