Sun Capsule, Inc. is one of 4823 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.
FDA 510(k) Regulatory Record - Sun Capsule, Inc.
2 devices