# MolecuLight Inc

> Medical device manufacturer record on deviCERTS, compiled from public registries. MolecuLight Inc is a medical device manufacturer based in Canada, with 13 devices listed in FDA GUDID and EUDAMED (FDA Class II and I; EU Class IIa) as of 14 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/moleculight-inc>
- Country: Canada (from SRN)
- EUDAMED actor status: active
- Role: Manufacturer
- Registrations: EUDAMED
- EUDAMED SRN: CA-MF-000036119
- DUNS: 202822052

## Figures

- Devices: 13
- FDA recalls (matched to the firm by name): 0

## Registry facts

*Every device of the manufacturer. A device listed in two registries counts in both.*

- Registries: FDA GUDID 12, EUDAMED 2
- Device classes: FDA Class II 9, EU Class IIa 2, FDA Class I 2
- EMDN [Z12 Instruments for functional explorations and therapeutic interventions](https://devicerts.com/categories/emdn/Z12): 2 devices

## Sites and related companies

- Authorised representative: [Emergo Europe B.V.](https://devicerts.com/representatives/emergo-europe-bv-nl-ar-000000116) (Netherlands)

## Devices

The first 13 of 13, in the order of the canonical page, which lists them all.

- [MolecuLightDX®+ Essential System 3155](https://devicerts.com/devices/moleculightdx-r-essential-system-3155) · Class II · GUDID · status: Active
- [MolecuLightDX Sterile Surgical Sleeve Convenience Kit of 25 2096](https://devicerts.com/devices/moleculightdx-sterile-surgical-sleeve-convenience-kit-of-25-2096) · Class II · GUDID · status: Listed
- [MolecuLightDX®+ Enterprise System 2635](https://devicerts.com/devices/moleculightdx-r-enterprise-system-2635) · Class II · GUDID · status: Active
- [Thermal Imaging Module 2640](https://devicerts.com/devices/thermal-imaging-module-2640) · Class I · GUDID · status: Listed
- [MolecuLightDX DarkDrape Eco Clip 2393](https://devicerts.com/devices/moleculightdx-darkdrape-eco-clip-2393) · Class II · GUDID · status: Listed
- [MolecuLightDX Eco DarkDrapes (Case of 50) 2517](https://devicerts.com/devices/moleculightdx-eco-darkdrapes-case-of-50-2517) · Class II · GUDID · status: Listed
- [MolecuLightDX+ Thermal Eco Clip 2395](https://devicerts.com/devices/moleculightdx-thermal-eco-clip-2395) · Class I · GUDID · status: Listed
- [i:X Sterile Surgical Sleeve Convenience Kit 1859](https://devicerts.com/devices/i-x-sterile-surgical-sleeve-convenience-kit-1859) · Class II · GUDID · status: Listed
- [MolecuLightDX System 2094](https://devicerts.com/devices/moleculightdx-system-2094) · Class II · GUDID · status: Active
- [MolecuLight DarkDrape 1426](https://devicerts.com/devices/moleculight-darkdrape-1426) · Class II · GUDID · status: Listed
- [MolecuLight i:X System 1153-11](https://devicerts.com/devices/moleculight-i-x-system-1153-11) · Class II · GUDID · status: Active
- [MolecuLight i:X](https://devicerts.com/devices/moleculight-i-x-1105) · ref 1105 · Class IIa · EUDAMED · status: Active
- [MolecuLightDX](https://devicerts.com/devices/moleculightdx-1594) · ref 1594 · Class IIa · EUDAMED, GUDID · status: Active

## Source and citation

- Cite as: MolecuLight Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/moleculight-inc (data as of 2026-11-14).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID](https://accessgudid.nlm.nih.gov/)
- EUDAMED record synced: 2026-11-07
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-14
- JSON: <https://devicerts.com/manufacturers/moleculight-inc.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/manufacturers/moleculight-inc
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.