Densitas, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Densitas, Inc. - FDA 510(k) Cleared Devices
Recent clearances: densitas densityai, DM-Density
2
Total
2
Cleared
0
Denied
Densitas, Inc. has 2 FDA 510(k) cleared medical devices. Based in Halifax, CA.
Historical record: 2 cleared submissions from 2018 to 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Densitas, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergogroup, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Densitas, Inc.
2 devices