K250833
- 510(k) number
- K250833
- Device name
- SwissMembrane X; SwissMembrane X Socket
- Applicant
- Geistlich Pharma AG CH
- Product code
- NPL — Barrier, Animal Source, Intraoral
- Decision date
- 2025-04-15
- Date received
- 2025-03-19
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K250833.pdf
Official FDA record: K250833
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.