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Trumatch

FDA UDI

Class II (US FDA UDI)

by Materialise NV

Identity

Trade Name
TRUMATCH FDA UDI
Generic Name
Craniofacial fixation plate kit, non-bioabsorbable FDA UDI
Device Name
TRUMATCH TI Implant - Midface Large FDA UDI
Model / Reference
SD980.105 FDA UDI
Description
TRUMATCH TI Implant - Midface Large FDA UDI

Identifiers

Catalog Number
SD980.105 FDA UDI
Primary DI / UDI-DI
05420060381058 FDA UDI
510(k) Number
K173039 FDA UDI
FDA Product Code
JEY FDA UDI
GMDN Term
Craniofacial fixation plate kit, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4760 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Craniofacial fixation plate kit, non-bioabsorbable

Trumatch by Materialise NV — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniofacial fixation plate kit, non-bioabsorbable.

Cleared under the same submission

K173039 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Materialise NV

Sources (1)

  • FDA UDI c1ac437e-13c4-47da-98fa-6ca3e1847e67 35 fields · synced May 31, 2026