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Axiom

FDA UDI

Class II (US FDA UDI)

by Etablissements Anthogyr

Identity

Trade Name
Axiom FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
HEALING SCREW Ø6.0 H3 Sealing of implant conical connection during bone healing. Preparing gingiva to the permanent restoration shape. FDA UDI
Model / Reference
OPHS630 FDA UDI
Description
HEALING SCREW Ø6.0 H3 Sealing of implant conical connection during bone healing. Preparing gingiva to the permanent restoration shape. FDA UDI

Identifiers

Primary DI / UDI-DI
03663394001472 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 6.0 Millimeter FDA UDI

Category: Dental implant suprastructure, temporary, preformed, single-use

Axiom by Etablissements Anthogyr — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1b9874b7-0481-4644-b1a5-c56e448021d9 36 fields · synced Jun 8, 2026