Teknor Medical Products, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Teknor Medical Products, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Teknor Medical Products, Inc. has 2 FDA 510(k) cleared medical devices. Based in Trenton, Ontario, CA.
Historical record: 2 cleared submissions from 1993 to 1993. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Teknor Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Teknor Medical Products, Inc.
2 devices