Kindel & Anderson is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kindel & Anderson - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Kindel & Anderson has 4 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 4 cleared submissions from 1980 to 1982. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Kindel & Anderson Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kindel & Anderson
4 devices