Sun Capsule, Inc. is one of 14497 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sun Capsule, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Sun Capsule, Inc. has 2 FDA 510(k) cleared medical devices. Based in Danvers, US.
Historical record: 2 cleared submissions from 1987 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sun Capsule, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aegis Regulatory, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Sun Capsule, Inc.
2 devices