Paragon Medical, Inc. is one of 18502 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Paragon Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Advanced Imaging Modality (AIM) Sterilization Tray, Endoscope and Camera Sterilization Tray, Camera Sterilization Tray, PARAGON MEDICAL SURGICAL INSTRUMENT DELIVERY SYSTEM VARIOUS
2
Total
2
Cleared
0
Denied
Paragon Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Fort Wayne, US.
Historical record: 2 cleared submissions from 2003 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Paragon Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Paragon Medical, Inc.
2 devices