Kirkstil Corp., Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Kirkstil Corp., Inc. has 3 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Historical record: 3 cleared submissions from 1985 to 1985. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Kirkstil Corp., Inc. Filter by specialty or product code using the sidebar.
3 devices