Biomerics is one of 12964 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomerics - FDA 510(k) Cleared Devices
Recent clearances: Vesta RF Cannula, NIMBUS ELECTROSURGICAL RADIOFREQUENCY MULTITINED EXPANDABLE ELECTRODE
2
Total
2
Cleared
0
Denied
Biomerics has 2 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 2 cleared submissions from 2012 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Biomerics Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Biomerics
2 devices