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ST Temporalis

FDA UDI

Class II (US FDA UDI)

by Osteosymbionics, LLC

Identity

Trade Name
ST Temporalis FDA UDI
Generic Name
Chin prosthesis FDA UDI
Device Name
Silicone Temporal Implant - Large FDA UDI
Model / Reference
STT-60 FDA UDI
Description
Silicone Temporal Implant - Large FDA UDI

Identifiers

Primary DI / UDI-DI
00866453000147 FDA UDI
510(k) Number
K111069 FDA UDI
FDA Product Code
MNF FDA UDI
GMDN Term
Chin prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3550 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Chin prosthesis

ST Temporalis by Osteosymbionics, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chin prosthesis.

Cleared under the same submission

K111069 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ed81a1ae-18f5-4d47-b0b9-35968914abc2 34 fields · synced May 30, 2026