Diotech CO is one of 18397 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diotech CO - FDA 510(k) Cleared Devices
Recent clearances: ATOVEN-Reusable Laser Fiber, DIOTECH LASER FIBER
2
Total
2
Cleared
0
Denied
Diotech CO has 2 FDA 510(k) cleared medical devices. Based in Pittsburgh, US.
Historical record: 2 cleared submissions from 2014 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Diotech CO Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Plusglobal as regulatory consultant.
FDA 510(k) Regulatory Record - Diotech CO
2 devices