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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
Dental prosthesis/implant abutment screw FDA UDI
Device Name
Abutment Screw - Anodized Purple (1.25mm/.050"hex drive) FDA UDI
Model / Reference
AS-P FDA UDI
Description
Abutment Screw - Anodized Purple (1.25mm/.050"hex drive) FDA UDI

Identifiers

Catalog Number
AS-P FDA UDI
Primary DI / UDI-DI
D896ASP0 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental prosthesis/implant abutment screw 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental prosthesis/implant abutment screw

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

Similar devices

Also classified as Dental prosthesis/implant abutment screw.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 944c58d3-45b8-4f80-b3f7-aca84e170541 35 fields · synced May 30, 2026