Vydence is one of 50 FDA 510(k) medical device manufacturers from Brazil in the dataset, ranked by real submission volume.
Vydence - FDA 510(k) Cleared Devices
Recent clearances: Siberian Fit
1
Total
1
Cleared
0
Denied
Vydence has 1 FDA 510(k) cleared medical devices. Based in Ceat - Sao Carlos/Sp Sao Paulo, BR.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vydence Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kathy Maynor as regulatory consultant.
FDA 510(k) Regulatory Record - Vydence
1 devices