Oryx Dental Software, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Oryx Dental Software, Inc. has 1 FDA 510(k) cleared medical devices. Based in Seattle, US.
Last cleared in 2022. Active since 2022. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Oryx Dental Software, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Oryx Dental Software, Inc.
1 devices