Moleculight, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
1
Denied
Moleculight, Inc. has 4 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Last cleared in 2022. Active since 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Moleculight, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Moleculight, Inc.
5 devices
Cleared
May 18, 2022
MolecuLight I:X
General & Plastic Surgery
160d
Cleared
Jul 21, 2021
MolecuLightDX
General & Plastic Surgery
30d
Cleared
Jun 22, 2021
MolecuLight I:X
General & Plastic Surgery
89d
Cleared
Dec 04, 2019
MolecuLight i:X
General & Plastic Surgery
196d
Not Cleared
Jul 31, 2018
MolecuLight i:X
General & Plastic Surgery
165d