Medskin Solutions Dr. Suwelack AG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Medskin Solutions Dr. Suwelack AG - FDA 510(k) Cleared Devices
Recent clearances: MatriDerm, MatriDerm pluS+ Bi-Layer, MatriDerm
3
Total
3
Cleared
0
Denied
Medskin Solutions Dr. Suwelack AG has 3 FDA 510(k) cleared medical devices. Based in Billerbeck, DE.
Latest FDA clearance: May 2026. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medskin Solutions Dr. Suwelack AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Secure BioMed Evaluations as regulatory consultant.
FDA 510(k) Regulatory Record - Medskin Solutions Dr. Suwelack AG
3 devices