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Kinn Automatic Volume Management System KIT-0002

by Vessl Prosthetics 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00628774388058 UDI-DI Date2 Mar 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  • Withdrawn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
Kinn Automatic Volume Management System
Generic Name
External lower-limb prosthesis structural/alignment component
Model / Reference
KIT-0002
Primary DI / UDI-DI
00628774388058
GMDN Term
External lower-limb prosthesis structural/alignment component
GUDID distribution status
In Commercial Distribution

Other devices from Vessl Prosthetics Inc

See all devices from Vessl Prosthetics Inc →

Properties

  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Serial Number

Other properties (10)

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