# BOTISS BIOMATERIALS GMBH

FEI: 3014206569
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Export Device to the United States But Perform No Other Operation on Device; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: botiss biomaterials GmbH (#10058419)

Address: Hauptstrasse 28, Zossen Brandenburg, 15806, DE

Mandatory US Agent: Registrar Corp

## Products

Total registered: 1
Top product codes: NPM
Regulation §: 872.3930

Proprietary names: Straumann cerabone, cerabone

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223014206569%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3014206569