Enzysurge , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Enzysurge , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: SilverStream Gel
3
Total
3
Cleared
0
Denied
Enzysurge , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Somerset, US.
Historical record: 3 cleared submissions from 2006 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Enzysurge , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bioreg Services as regulatory consultant.
FDA 510(k) Regulatory Record - Enzysurge , Ltd.
3 devices