Matricel GmbH

FDA Device Registration & Listing · Herzogenrath North Rhine-Westphalia, DE · Registration 3019834892

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3019834892
FEI Number
3019834892
Entity Name
Matricel GmbH
City/State/Country
Herzogenrath North Rhine-Westphalia, DE
Establishment Address
Konrad-Zuse-Strasse 6, Herzogenrath North Rhine-Westphalia 52134, DE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Matricel GmbH (Owner Number: 10026736)
Owner / Operator Contact Address
Kaiserstrasse 100, Herzogenrath, DE-NW 52134, DE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K123697
PMA Number
N/A

All Registered Proprietary Names

creos xenoprotect Kontour Matrix Zmatrix

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NPL Barrier, Animal Source, Intraoral Dental Class 2 872.3930 2014-04-28

Official Correspondent

Leon Olde Damink

US Agent Details

John Sharobiem Email: john.sharobiem@envistaco.com Phone: (732) 3958085

Related Public Records

Same Entity

Matricel GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3007113424 MATRICEL GMBH Herzogenrath North Rhine-Westphalia, DE

Similar Registrations

Registration Number Establishment Name Location
3043657402 NEO MODULUS (SUZHOU) MEDICAL SCI-TECH CO., LTD. Suzhou City Jiangsu, CN
3014015147 ORTHOCELL LIMITED Perth Western Australia, AU
3014206569 BOTISS BIOMATERIALS GMBH Zossen Brandenburg, DE
3027448274 Collagen Matrix, Inc. Mahwah, NJ, US
1319660 ISOMEDIX OPERATIONS INC. CHESTER, NY, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3019834892. Last updated year: 2026. Please use registration number 3019834892 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.