Cybermed, Inc. is one of 17560 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cybermed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CORE1 Implant System, ONDEMAND3D, ONDEMAND3D
6
Total
6
Cleared
0
Denied
Cybermed, Inc. has 6 FDA 510(k) cleared medical devices. Based in San Leandro, US.
Last cleared in 2022. Active since 2001. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Cybermed, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Cybermed, Inc.
6 devices