Kalera Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kalera Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Kalera Vacuum Aspiration Catheter (K-VAC)
1
Total
1
Cleared
0
Denied
Kalera Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Kalera Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kalera Medical, Inc.
1 devices