Bioptron AG is one of 25333 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bioptron AG - FDA 510(k) Cleared Devices
Recent clearances: BIOPTRON PRO LIGHT THERAPY SYSTEM AND BIOPTRON COMPACT III LIGHT THERAPY SYSTEM
1
Total
1
Cleared
0
Denied
Bioptron AG has 1 FDA 510(k) cleared medical devices. Based in Littleton, US.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Bioptron AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioptron AG
1 devices