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Astra Tech Implant System® 24685

by Dentsply Implants Manufacturing GmbH

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 Number07392532070327 UDI-DI Date19 Oct 2023ListedStatusListed 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  • Withdrawn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
Astra Tech Implant System®
Generic Name
Orthopaedic osteotome
Model / Ref / Catalog
24685
Description
Osteotome 4.2/4.7 Round, Straight
Primary DI / UDI-DI
07392532070327
FDA Product Code
NDP
GMDN Term
Orthopaedic osteotome
Device Class
Class I
Regulation Number
872.3980
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic osteotome

Other devices from Dentsply Implants Manufacturing GmbH

See all devices from Dentsply Implants Manufacturing GmbH →

Properties

  • Premarket Exempt
  • Lot / Batch Number

Other properties (12)

  • 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
  • Manufacturing Date: No