Osyris is one of 295 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Osyris - FDA 510(k) Cleared Devices
Recent clearances: SMOOTHKIT+, PHARAON 980 ENDO/EXO, OSYFIBRE 600, CONTROL4+ HANDPIECE, PHARAON LIPO
3
Total
3
Cleared
0
Denied
Osyris has 3 FDA 510(k) cleared medical devices. Based in Hellemmes, FR.
Historical record: 3 cleared submissions from 2008 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Osyris Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Osyris
3 devices