Trigen

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: TRIGEN FDA UDI
Generic Name: Stereotactic surgery system probe, single-use FDA UDI
Device Name: SURESHOT META STANDARD DRILL GUIDE PROBE FDA UDI
Model / Reference: 71692814 FDA UDI
Description: SURESHOT META STANDARD DRILL GUIDE PROBE FDA UDI

Identifiers

Catalog Number: 71692814 FDA UDI
Primary DI / UDI-DI: 03596010648143 FDA UDI
510(k) Number: K092497 FDA UDI
FDA Product Code: OLO FDA UDI
GMDN Term: Stereotactic surgery system probe, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.4560 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Stereotactic surgery system probe, single-use

Trigen by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K092497 also covers:

TRIGEN — Smith & Nephew, Inc.

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 II	Pending data

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Manufacturer

Manufacturer: Smith & Nephew, Inc.

Sources (1)

FDA UDI 20534fb1-0368-4916-af80-ec3f5ed008f6 36 fields · synced Jun 8, 2026