Provide®

FDA UDI

Class I (US FDA UDI)

by Biomet 3i, Llc

Identity

Trade Name: PROVIDE® FDA UDI
Generic Name: Dental implant analog FDA UDI
Device Name: PROVIDE® ABUTMENT ANALOG WITH PIN 6.5MM(P) FDA UDI
Model / Reference: PAAP65 FDA UDI
Description: PROVIDE® ABUTMENT ANALOG WITH PIN 6.5MM(P) FDA UDI

Identifiers

Primary DI / UDI-DI: 00844868013648 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Dental implant analog 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

Yes

FDA UDI

Over-the-Counter

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

FDA UDI

Category: Dental implant analog

Provide® by Biomet 3i, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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DYNAMIC ABUTMENT® SOLUTIONS — TALLADIUM ESPAÑA SL · Class I
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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: Biomet 3i, Llc

Sources (1)

FDA UDI 8caacd68-cdf8-44f4-bc4d-937ad62b6b1d 34 fields · synced May 30, 2026