Prosthetic devices · 21 CFR 872 Subpart D
Polytetrafluoroethylene Vitreous Carbon Materials for Maxillofacial Alveolar Ridge Augmentation
FDA device type “Materials, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Alveolar Ridge Augmentation”.
- Companies listing it
- 00 makers
- Brands and models
- 0
- 510(k) clearances
- 00 in five years
- FDA name
- Materials, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Alveolar Ridge Augmentation
Official records: FDA product classification for NFE · 21 CFR 872.3680.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026