Medtek Devices, Inc. is one of 20302 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtek Devices, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PLUMEPEN INTEGRATED SMOKE EVACUATION PENCIL, LAPEVAC, FILTRATION DEVICE FOR THE PERIOTONEUM
2
Total
2
Cleared
0
Denied
Medtek Devices, Inc. has 2 FDA 510(k) cleared medical devices. Based in Buffalo, US.
Historical record: 2 cleared submissions from 2006 to 2011. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medtek Devices, 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 - Medtek Devices, Inc.
2 devices