Clearance Summary
Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide® received FDA 510(k) clearance under submission number K252253, sponsored by Geistlich Pharma AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2025-11-25.
- Submission: K252253
- Applicant / Sponsor: Geistlich Pharma AG
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3930
- Decision date: 2025-11-25
Classification & Regulation
This clearance is catalogued under FDA product code NPL and 21 CFR 872.3930, within the Dental review panel as a Class II device.