Data / Medical devices / Germany / Matricel GMBH
Matricel GMBH: FDA-registered device maker in Herzogenrath North Rhine-Westphalia, Germany, 1 510(k) clearance
Matricel GMBH is registered with the FDA (registration 3007113424) in Herzogenrath North Rhine-Westphalia, Germany. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 24, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007113424
- Address
- Kaiserstrasse 100, Herzogenrath North Rhine-Westphalia, Germany, 52134
- Owner or operator
- Matricel GmbH (10026736)
- Roles
- Manufacturer
- First device listed
- April 28, 2014
- Registered through
- 2026
- Brand names listed
- Kontour Matrix, Zmatrix, creos xenoprotect
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Barrier, Animal Source, Intraoral | NPL | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 24, 2014 | K123697 | MATRICEL DENTAL BARRIER MEMBRANE | NPL | Substantially Equivalent | Matricel GmbH | accessdata.fda.gov |
Compare with other makers
Updated February 24, 2014. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.