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STAR PSI Talus Cut Guide

FDA UDI

Class III (US FDA UDI)

by Trilliant Surgical LLC

Identity

Trade Name
STAR PSI Talus Cut Guide FDA UDI
Generic Name
Custom-made orthopaedic/craniofacial surgical guide FDA UDI
Model / Reference
601-02-000 FDA UDI

Identifiers

Primary DI / UDI-DI
00810028393455 FDA UDI
PMA Number
P050050 FDA UDI
FDA Product Code
NTG FDA UDI
GMDN Term
Custom-made orthopaedic/craniofacial surgical guide FDA UDI

Classification

Device Class
Class III 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Custom-made orthopaedic/craniofacial surgical guide

STAR PSI Talus Cut Guide by Trilliant Surgical LLC — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Custom-made orthopaedic/craniofacial surgical guide.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 06f88c75-6636-4356-947d-db8996cbbdb5 33 fields · synced May 30, 2026