Presthetic Accessories

FDA UDI

Class II (US FDA UDI)

by A.b. Dental Devices Ltd

Identity

Trade Name: Presthetic Accessories FDA UDI
Generic Name: Dental implant suprastructure kit FDA UDI
Device Name: Titanium Healing Cap, 3 mm Diameter, 4 mm length FDA UDI
Model / Reference: P0-3,4 FDA UDI
Description: Titanium Healing Cap, 3 mm Diameter, 4 mm length FDA UDI

Identifiers

Catalog Number: P0-3,4 FDA UDI
Primary DI / UDI-DI: 07290107271349 FDA UDI
FDA Product Code: NHA FDA UDI
GMDN Term: Dental implant suprastructure kit 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

FDA UDI

Single Use

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 3 Millimeter FDA UDI

Category: Dental implant suprastructure kit

Presthetic Accessories by A.b. Dental Devices Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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KLOCKNER — SOADCO, S.L. · Class II

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 II	Pending data

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Manufacturer

Manufacturer: A.b. Dental Devices Ltd

Sources (1)

FDA UDI 97ece14b-7e16-4a62-9ae4-4dcfbda572b9 36 fields · synced Jun 1, 2026