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Lab prosthetic screw J4013.2001

by ALTATEC GmbH 2 variants

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 Number04099797997583 UDI-DI Date17 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  • Withdrawn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
Lab prosthetic screw
Generic Name
Dental implant abutment analog, laboratory
Model / Ref / Catalog
J4013.2001
Primary DI / UDI-DI
04099797997583
FDA Product Code
NDP
GMDN Term
Dental implant abutment analog, laboratory
Device Class
Class I
Regulation Number
872.3980
GUDID distribution status
In Commercial Distribution

Other devices from ALTATEC GmbH

See all devices from ALTATEC GmbH →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

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