Medegen, Inc. is one of 24980 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medegen, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MEDEGEN PRESSURE RATED EXTENSION SETS
1
Total
1
Cleared
0
Denied
Medegen, Inc. has 1 FDA 510(k) cleared medical devices. Based in Ontario, US.
Historical record: 1 cleared submissions from 2008 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medegen, 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 - Medegen, Inc.
1 devices