Oracrew is one of 20575 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oracrew - FDA 510(k) Cleared Devices
Recent clearances: CompleClear Plastic Orthodontic Bracket and Wire Appliance
1
Total
1
Cleared
0
Denied
Oracrew has 1 FDA 510(k) cleared medical devices. Based in Las Vegas, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Oracrew Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Blackwell Device Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Oracrew
1 devices