Medical Device Manufacturer · US , Santa Clara , CA

Cemax, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1988

Total

Cleared

Denied

Cemax, Inc. has 7 FDA 510(k) cleared medical devices. Based in Santa Clara, US.

Historical record: 7 cleared submissions from 1988 to 1995. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Cemax, Inc. Filter by specialty or product code using the sidebar.

Cemax, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cemax, Inc.

7 devices

1-7 of 7