Opus Ksd, Inc. is one of 19310 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Opus Ksd, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SUBQ IT! BIOABSORBABLE SKIN CLOSURE SYSTEM
1
Total
1
Cleared
0
Denied
Opus Ksd, Inc. has 1 FDA 510(k) cleared medical devices. Based in Marlborough, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Opus Ksd, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Aptiv Solutions as regulatory consultant.
FDA 510(k) Regulatory Record - Opus Ksd, Inc.
1 devices