Canadian Pioneer Medical Technology Corporation is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Canadian Pioneer Medical Technology Corporation - FDA 510(k) Cleared ...
Recent clearances: Laser treatment system , models Nyx plus, Grace plus, Nemesis, Ares, Laser Treatment System, Model: Hera, Armo, Laser Treatment System, Model: NYX and Grace
3
Total
3
Cleared
0
Denied
Canadian Pioneer Medical Technology Corporation has 3 FDA 510(k) cleared medical devices. Based in Vaughan, CA.
Last cleared in 2022. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Canadian Pioneer Medical Technology Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Canadian Pioneer Medical Technology Corporation
3 devices
Cleared
Feb 25, 2022
Laser treatment system , models Nyx plus, Grace plus, Nemesis, Ares
General & Plastic Surgery
266d
Cleared
Oct 25, 2021
Laser Treatment System, Model: Hera, Armo
General & Plastic Surgery
54d
Cleared
Feb 26, 2021
Laser Treatment System, Model: NYX and Grace
General & Plastic Surgery
52d