← Back to catalogue

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 drilling system attachment FDA UDI
Device Name
Latch Type Handpiece Connector (4mm Square Drive System) FDA UDI
Model / Reference
4DHPC FDA UDI
Description
Latch Type Handpiece Connector (4mm Square Drive System) FDA UDI

Identifiers

Catalog Number
4DHPC FDA UDI
Primary DI / UDI-DI
D8964DHPC0 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental drilling system attachment 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

No

FDA UDI

Implantable

No

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 drilling system attachment

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 drilling system attachment.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
American Dental Implant Corporation

Sources (1)

  • FDA UDI 04e24bd6-0c3c-498b-ac63-8808899e3a7a 35 fields · synced May 29, 2026