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Titan Implants Inc.

FDA UDI

Class I (US FDA UDI)

by Titan Implant Inc

Identity

Trade Name
TITAN IMPLANTS INC. FDA UDI
Generic Name
Dental implant abutment analog, laboratory FDA UDI
Device Name
6.5mm TG Hex Abutment Analog FDA UDI
Model / Reference
TN2-65TGHAA-AL FDA UDI
Description
6.5mm TG Hex Abutment Analog FDA UDI

Identifiers

Primary DI / UDI-DI
00842448115560 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant abutment analog, laboratory 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

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

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

No

FDA UDI

Category: Dental implant abutment analog, laboratory

Titan Implants Inc. by Titan Implant Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant abutment analog, laboratory.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Titan Implant Inc

Sources (1)

  • FDA UDI f2f649f7-1bb0-4f49-a996-3c1d241be8ba 33 fields · synced Jun 8, 2026