FDA Device Establishments · JSON-LD · Markdown

BOTISS BIOMATERIALS GMBH

FEI 3014206569 · 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 · Status: Active

FEI Number3014206569
Owner / Operatorbotiss biomaterials GmbH (#10058419)
AddressHauptstrasse 28, Zossen Brandenburg, 15806, DE
Mandatory US AgentRegistrar Corp
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)NPM
Regulation § (21 CFR)872.3930
Proprietary namesStraumann cerabone; cerabone

External sources

Source: openFDA. Public-domain (CC0).