Koya, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Koya, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Koya Ripple
1
Total
1
Cleared
0
Denied
Koya, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Koya, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Koya, Inc.
1 devices