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Kinos Aeros Instrumentation 5871-0018

by Restor3D

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

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 Number00840097513188 UDI-DI Date9 Apr 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Kinos Aeros Instrumentation
Generic Name
Joint prosthesis implantation kit, reusable
Model / Reference
5871-0018
Primary DI / UDI-DI
00840097513188
510(k) Number
FDA Product Code
HSN
GMDN Term
Joint prosthesis implantation kit, reusable
Device Class
Class II
Regulation Number
888.3110
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K242868)

Show all (12)

Other devices from Restor3D

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No