← Back to catalogue

Kontour Matrix

FDA UDI

Class II (US FDA UDI)

by Matricel GmbH

Identity

Trade Name
Kontour Matrix FDA UDI
Generic Name
Collagen dental regeneration membrane FDA UDI
Device Name
Collagen membrane FDA UDI
Model / Reference
KMAX3040 FDA UDI
Description
Collagen membrane FDA UDI

Identifiers

Primary DI / UDI-DI
04250830900643 FDA UDI
510(k) Number
K123697 FDA UDI
FDA Product Code
NPL FDA UDI
GMDN Term
Collagen dental regeneration membrane FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3930 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

Dimensions & Sizes

Size
Area/Surface Area — 1200 Square millimeter FDA UDI

Category: Collagen dental regeneration membrane

Kontour Matrix by Matricel GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Collagen dental regeneration membrane.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Matricel GmbH

Sources (1)

  • FDA UDI ffab2653-f9da-459d-b30e-e7705ab3c491 37 fields · synced May 30, 2026