B-Temia, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
B-Temia, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Keeogo Dermoskeleton System
1
Total
1
Cleared
0
Denied
B-Temia, Inc. has 1 FDA 510(k) cleared medical devices. Based in St-Augustin-De-Desmaures, CA.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by B-Temia, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Covington & Burling, Llp as regulatory consultant.
FDA 510(k) Regulatory Record - B-Temia, Inc.
1 devices