Axiom®

FDA UDI

Class I (US FDA UDI)

by Etablissements Anthogyr

Identity

Trade Name: AXIOM® FDA UDI
Generic Name: Dental drill bit extension FDA UDI
Device Name: GUIDED IMPL MDRL BL G4.2 L FDA UDI
Model / Reference: GMVG42L FDA UDI
Description: GUIDED IMPL MDRL BL G4.2 L FDA UDI

Identifiers

Primary DI / UDI-DI: 03663394484992 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Dental drill bit extension FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3980 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 39.700000000000003 Millimeter FDA UDI
Outer Diameter — 4 Millimeter FDA UDI

Category: Dental drill bit extension

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

Similar devices

Also classified as Dental drill bit extension.

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Zuga — Zuga Medical, Inc. · Class II
Restore — Keystone Dental Inc. · Class II
Drill Extension — Ossvis Co., Ltd. · Class I
A. Titan Instruments — A.Titan Instruments · Class I
Tapered Screw-Vent® — ZIMMER DENTAL INC. · Class I
Mount Extension — POINTIMPLANT Co., Ltd. · Class I
Tapered Screw-Vent® — ZIMMER DENTAL INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Etablissements Anthogyr

Sources (1)

FDA UDI 6f15c66e-d291-4721-be7e-5fa81a8a1d17 34 fields · synced May 30, 2026