Orifice Medical AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Orifice Medical AB - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Orifice Medical AB has 2 FDA 510(k) cleared medical devices. Based in Ystad, SE.
Historical record: 2 cleared submissions from 1999 to 1999. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Orifice Medical AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Orifice Medical AB
2 devices