K252253
- 510(k) number
- K252253
- Device name
- Geistlich Mucograft® /Geistlich Mucograft® Seal; Geistlich Fibro-Gide®
- Applicant
- Geistlich Pharma AG CH
- Product code
- NPL — Barrier, Animal Source, Intraoral
- Decision date
- 2025-11-25
- Date received
- 2025-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K252253.pdf
Official FDA record: K252253
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.