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Axiom OPSC010

by Etablissements Anthogyr

Axiom OPSC010 is a Class II device made by Etablissements Anthogyr, listed in FDA GUDID since 31 Jul 2015 (UDI-DI 03663394001823), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number03663394001823 UDI-DI Date31 Jul 2015ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Axiom
Generic name
Dental implant suprastructure, permanent, preformed
Model / reference
OPSC010
Description
CONICAL ABUTMENT 0° H1 Providing support for a permanent restoration
Primary DI / UDI-DI
03663394001823
FDA product code
NHA
GMDN term
Dental implant suprastructure, permanent, preformed
Device class
Class II
Regulation number
872.3630
GUDID distribution status
In Commercial Distribution
Size
Angle — 0 degree

Related devices

Category: Dental implant suprastructure, permanent, preformed

Similar devices in this category

Other devices filed under Dental implant suprastructure, permanent, preformed.

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)