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Tg Osseotite®

FDA UDI

Class I (US FDA UDI)

by Biomet 3i, Llc

Identity

Trade Name
TG OSSEOTITE® FDA UDI
Generic Name
Fixture/appliance dental drill bit, reusable FDA UDI
Device Name
TG OSSEOTITE® 2/3MM PILOT DRILL FDA UDI
Model / Reference
PSD100 FDA UDI
Description
TG OSSEOTITE® 2/3MM PILOT DRILL FDA UDI

Identifiers

Primary DI / UDI-DI
00844868014539 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Fixture/appliance dental drill bit, reusable 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

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: Fixture/appliance dental drill bit, reusable

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

Similar devices

Also classified as Fixture/appliance dental drill bit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biomet 3i, Llc

Sources (1)

  • FDA UDI 194f6110-917b-4fe2-9d78-88db2e8cf650 34 fields · synced May 30, 2026