Arthromeda, Inc. is one of 18467 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arthromeda, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ArthroPlan Digital Templating Software
1
Total
1
Cleared
0
Denied
Arthromeda, Inc. has 1 FDA 510(k) cleared medical devices. Based in Lowell, US.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Arthromeda, Inc. 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 - Arthromeda, Inc.
1 devices