American Dental Implant

FDA UDI

Class I (US FDA UDI)

by American Dental Implant Corporation

Identity

Trade Name: American Dental Implant FDA UDI
Generic Name: Surgical screwdriver, reusable FDA UDI
Device Name: 1.25mm / .050" Hex Finger Driver FDA UDI
Model / Reference: FD050 FDA UDI
Description: 1.25mm / .050" Hex Finger Driver FDA UDI

Identifiers

Catalog Number: FD050 FDA UDI
Primary DI / UDI-DI: D896FD0500 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Surgical screwdriver, reusable 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

FDA UDI

Over-the-Counter

Yes

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

Category: Surgical screwdriver, reusable

American Dental Implant by American Dental Implant Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: American Dental Implant Corporation

Sources (1)

FDA UDI 15de01cc-930e-477b-84f8-6f5e5780e167 35 fields · synced Jun 6, 2026