Anglefix is one of 20709 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Anglefix - FDA 510(k) Cleared Devices
Recent clearances: ANGLEFIX T LOCKING PLATE, MODELS AF-001 (PLATE), ST-1 (LOCKING SCREW)
1
Total
1
Cleared
0
Denied
Anglefix has 1 FDA 510(k) cleared medical devices. Based in Apple Valley, US.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Anglefix Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Anglefix
1 devices