Koya Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Koya Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Dayspring, Dayspring Lite, Dayspring
3
Total
3
Cleared
0
Denied
Koya Medical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Oakland, US.
Latest FDA clearance: Jan 2024. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Koya Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Biodesign Regulatory Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Koya Medical, Inc.
3 devices