Oscimed SA is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Oscimed SA - FDA 510(k) Cleared Devices
Recent clearances: Aniti-Snore Mouthguard+
1
Total
1
Cleared
0
Denied
Oscimed SA has 1 FDA 510(k) cleared medical devices. Based in Suisse, CH.
Latest FDA clearance: Jan 2024. Active since 2024. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Oscimed SA Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Rook Quality Systems as regulatory consultant.
FDA 510(k) Regulatory Record - Oscimed SA
1 devices