Belimed AG is one of 118 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Belimed AG - FDA 510(k) Cleared Devices
Recent clearances: Belimed Steam Sterilizer MST-H TOP 5000, Belimed Steam Sterilizer MST-H TOP 5000
2
Total
2
Cleared
0
Denied
Belimed AG has 2 FDA 510(k) cleared medical devices. Based in Zug, CH.
Historical record: 2 cleared submissions from 2017 to 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Belimed AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Belimed, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Belimed AG
2 devices