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MolecuLight Inc

Canada·CA-MF-000036119

Last updated May 25, 2026

What MolecuLight Inc makes

MolecuLight Inc manufactures fluorescence wound imaging units and patient surgical drapes, including the MolecuLightDX System, MolecuLight i:X System, and MolecuLight DarkDrape.

The company's products are classified as Class II and Class IIa devices and are listed in the EU's EUDAMED and FDA's UDI databases. MolecuLight Inc is based in Canada.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What does MolecuLight Inc manufacture?

MolecuLight Inc manufactures fluorescence wound imaging units and patient surgical drapes, including the MolecuLightDX System, MolecuLight i:X System, and MolecuLight DarkDrape.

Where is MolecuLight Inc based?

MolecuLight Inc is based in Canada, as indicated by the country code CA in the device data.

Which regulatory registries list MolecuLight Inc's devices?

MolecuLight Inc's devices are listed in the EU's EUDAMED and the FDA's UDI databases, as specified in the device data.

How are MolecuLight Inc's devices classified?

MolecuLight Inc's devices are classified as Class II and Class IIa, which are regulatory classifications indicating the level of control required for safety and effectiveness.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Canada
Address
425 , University Avenue, Toronto, Canada
LinkedIn
—
Facebook
—
Phone
+1- 647 362 4684
PRRC Contact
Jordan John
EUDAMED SRN
CA-MF-000036119
FDA FEI Number
—
DUNS Number
202822052

Catalogue (6)

DeviceModel / ReferenceRegistriesClassStatus
i:X Sterile Surgical Sleeve Convenience Kit 1859
FDA UDI
Class IIActive
MolecuLightDX System 2094
FDA UDI
Class IIActive
MolecuLight DarkDrape 1426
FDA UDI
Class IIActive
MolecuLight i:X System 1153-11
FDA UDI
Class IIActive
MolecuLight i:X 1105
EUDAMED
Class IIaActive
MolecuLightDX 1594
EUDAMEDFDA UDI
Class IIaActive

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