Benjamin Biomedical, Inc. is one of 25821 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Benjamin Biomedical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: BENJAMIN ENVOY PHACO HANDPIECE
1
Total
1
Cleared
0
Denied
Benjamin Biomedical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Appollo Beach, US.
Historical record: 1 cleared submissions from 2002 to 2002. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Benjamin Biomedical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Benjamin Biomedical, Inc.
1 devices