Omnia Spa is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Omnia Spa - FDA 510(k) Cleared Devices
Recent clearances: PTFE SURGICAL SUTURE
3
Total
3
Cleared
0
Denied
Omnia Spa has 3 FDA 510(k) cleared medical devices. Based in Carmel, US.
Historical record: 3 cleared submissions from 2011 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Omnia Spa Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by THEMA S.r.l. as regulatory consultant.
FDA 510(k) Regulatory Record - Omnia Spa
3 devices