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Implant-One

FDA UDI

Class II (US FDA UDI)

by Implant Logistics, Inc.

Identity

Trade Name
Implant-One FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Abutment, 300 Series Angled Post 2mm Cuff Height. Includes screw. FDA UDI
Model / Reference
APT-0320-30 FDA UDI
Description
Abutment, 300 Series Angled Post 2mm Cuff Height. Includes screw. FDA UDI

Identifiers

Primary DI / UDI-DI
D762APT0320300 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 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

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, permanent, preformed

Implant-One by Implant Logistics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 656087fd-10c7-4225-9283-155dee6dc1da 34 fields · synced Jun 1, 2026