Mcginley Innovations is one of 18553 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mcginley Innovations - FDA 510(k) Cleared Devices
Recent clearances: IntelliSense Drill
1
Total
1
Cleared
0
Denied
Mcginley Innovations has 1 FDA 510(k) cleared medical devices. Based in Casper, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Mcginley Innovations Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Mcginley Innovations
1 devices