Extension , Inc. is one of 5191 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Extension , Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Extension , Inc. has 1 FDA 510(k) cleared medical devices. Based in Beaverton, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Extension , Inc. Filter by specialty or product code using the sidebar.
Extension , Inc. — FDA 510(k) Products and Clearance History
1 devices