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Axiom®

FDA UDI

Class II (US FDA UDI)

by Etablissements Anthogyr

Identity

Trade Name
AXIOM® FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
AXIOM IMPLANT X3 Ø6.4 X 6.5 FDA UDI
Model / Reference
XT64060 FDA UDI
Description
AXIOM IMPLANT X3 Ø6.4 X 6.5 FDA UDI

Identifiers

Primary DI / UDI-DI
03663394483742 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Screw endosteal dental implant, two-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 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
Length — 6.5 Millimeter FDA UDI
Outer Diameter — 6.4 Millimeter FDA UDI

Category: Screw endosteal dental implant, two-piece

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

Similar devices

Also classified as Screw endosteal dental implant, two-piece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a6640dd0-46a7-487c-8b9d-9cc17f510546 34 fields · synced May 30, 2026