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FDA product code NFE

Materials, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Alveolar Ridge Augmentation

DentalClass 221 CFR 872.3680
Verified
US regulatory classifications
US Product Code (FDA)
NFE
View Product Code Classification
US Risk Class (FDA)
Class 2
US Regulation (CFR)
21 CFR 872.3680
View CFR Regulation
Medical specialty
Dental
Device characteristics
GMP exempt
No
Implantable
No
Life-sustaining
No
Third party review
Not Eligible
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01PTFE implant02Vitreous carbon03Alveolar augmentation04Maxillofacial graft05Bone graft06Dental implant07Ridge augmentation08Facial implant09Biomaterial10Graft material
About this record

Materials, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Alveolar Ridge Augmentation is a medical device type in the Dental specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.