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Matrixwave

FDA UDI

Class II (US FDA UDI)

by Synthes

Identity

Trade Name
MATRIXWAVE FDA UDI
Generic Name
Orthodontic anchor plate FDA UDI
Device Name
MATRIXWAVE MMF TI PLATE 10 HOLES/TALL FDA UDI
Model / Reference
04.503.821 FDA UDI
Description
MATRIXWAVE MMF TI PLATE 10 HOLES/TALL FDA UDI

Identifiers

Catalog Number
04503821 FDA UDI
Primary DI / UDI-DI
10887587069449 FDA UDI
510(k) Number
K141165 FDA UDI
FDA Product Code
JEY FDA UDI
GMDN Term
Orthodontic anchor plate 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthodontic anchor plate

Matrixwave by Synthes — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic anchor plate.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Synthes

Sources (1)

  • FDA UDI db442d9e-84b7-46bb-b592-aa1e07982be2 36 fields · synced Jun 1, 2026