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Sign in to claim this brandMatricel GmbH
US
Last updated May 30, 2026
What Matricel GmbH makes
Matricel GmbH produces collagen-based dental regeneration membranes designed to support tissue growth during bone or periodontal procedures. These include resorbable barriers like the creos™ xenoprotect, Zmatrix, and Kontour Matrix, which are used in guided tissue regeneration and socket preservation in dental surgery.
The company’s products are classified as Class II medical devices and are listed under FDA 510(k) and UDI registries. The manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Matricel GmbH manufacture?
Matricel GmbH specializes in collagen-based dental regeneration membranes. These products are primarily used as resorbable barriers in dental procedures to support tissue growth during bone or periodontal regeneration, such as guided tissue regeneration and socket preservation. Examples include creos™ xenoprotect, Zmatrix, and Kontour Matrix.
Where is Matricel GmbH based?
Matricel GmbH is based in the United States. The company’s focus is on developing and manufacturing collagen-based dental regeneration membranes tailored for surgical applications in dentistry.
Which regulatory registries list Matricel GmbH’s devices?
Matricel GmbH’s devices are listed in the FDA’s 510(k) premarket notification registry and the FDA’s Unique Device Identifier (UDI) system. These registries track Class II medical devices to ensure compliance with U.S. regulatory requirements.
How are Matricel GmbH’s devices classified under U.S. regulations?
Matricel GmbH’s collagen-based dental regeneration membranes are classified as Class II medical devices. This classification applies because they are intended for surgical use in dental procedures, where moderate risk is associated with their function and potential patient impact.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- matricel.com
- —
- —
- [email protected]
- Phone
- +49240756440
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 344166512
Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| creos™ xenoprotect | N3040 | FDA UDI | Class II | Active |
| Zmatrix | ZM1520 | FDA UDI | Class II | Active |
| Kontour Matrix | KMAX3040 | FDA UDI | Class II | Active |
| Zmatrix | ZM3040 | FDA UDI | Class II | Active |
| creos™ xenoprotect | N2530 | FDA UDI | Class II | Active |
| creos™ xenoprotect | N1520 | FDA UDI | Class II | Active |
| Kontour Matrix | KMAX2530 | FDA UDI | Class II | Active |
| Kontour Matrix | KMAX1520 | FDA UDI | Class II | Active |
| Zmatrix | ZM2530 | FDA UDI | Class II | Active |
| Matricel Dental Barrier Membrane | K123697 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Matricel Gmbh Herzogenrath North Rhine-Westphalia · DE FEI 3007113424