Medkey, LLC is one of 18402 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medkey, LLC - FDA 510(k) Cleared Devices
Recent clearances: DuraLazeTM HoLEP Laser Fiber
1
Total
1
Cleared
0
Denied
Medkey, LLC has 1 FDA 510(k) cleared medical devices. Based in Bloomington, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medkey, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Catheter Research, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Medkey, LLC
1 devices