T.E.S., Ltd. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
T.E.S., Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
T.E.S., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Kanata, Ontario, CA.
Historical record: 1 cleared submissions from 1997 to 1997. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by T.E.S., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - T.E.S., Ltd.
1 devices