# Neomedlight

> Medical device manufacturer record on deviCERTS, compiled from public registries. Neomedlight is a medical device manufacturer based in France, with 13 devices listed in EUDAMED, FDA GUDID and FDA 510(k) (EU Class I and IIa; FDA Class II) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/neomedlight>
- Country: France (from SRN)
- EUDAMED actor status: active
- Role: Manufacturer
- Registrations: EUDAMED, FDA
- EUDAMED SRN: FR-MF-000004044
- FDA FEI: 3013919653
- DUNS: 265910339

## 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: EUDAMED 10, FDA GUDID 10, FDA 510(k) 1
- Device classes: EU Class I 5, EU Class IIa 5, FDA Class II 3
- EMDN [Z12 Instruments for functional explorations and therapeutic interventions](https://devicerts.com/categories/emdn/Z12): 10 devices

## Devices

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

- [BiliCocoon™ Service Kit BCC010-SK10](https://devicerts.com/devices/bilicocoon-service-kit-bcc010-sk10-eec24513) · Class II · GUDID · status: Active
- [BiliCocoon™ Service Kit BCC010-SK10](https://devicerts.com/devices/bilicocoon-service-kit-bcc010-sk10) · Class II · GUDID · status: Active
- [BiliCocoon™ Bag Disposable - Small](https://devicerts.com/devices/bilicocoon-bag-disposable-small-bcc221-s) · ref BCC221-S · Class I · EUDAMED · status: Active
- [CareMin650 ™ Oral Sleeve](https://devicerts.com/devices/caremin650-oral-sleeve-cm211) · ref CM211 · Class I · EUDAMED · status: Active
- [Bilicocoon™ Phototherapy System](https://devicerts.com/devices/bilicocoon-phototherapy-system-lbi) · ref K163526 · Class II · 510(k) · status: Active · decision 2017-10-06
- [BiliCocoon™ Bag Disposable](https://devicerts.com/devices/bilicocoon-bag-disposable-bcc221) · ref BCC221 · Class I · EUDAMED, GUDID · status: Active
- [BiliCocoon™ Light Box](https://devicerts.com/devices/bilicocoon-light-box-bcc010) · ref BCC010 · Class IIa · EUDAMED, GUDID · status: Active
- [BiliCocoon™ Fixation System](https://devicerts.com/devices/bilicocoon-fixation-system-bcc301) · ref BCC301 · Class I · EUDAMED, GUDID · status: Active
- [BiliCocoon™ Nest Pad](https://devicerts.com/devices/bilicocoon-nest-pad-bcc111) · ref BCC111 · Class IIa · EUDAMED, GUDID · status: Active
- [BiliCocoon™ Nest System](https://devicerts.com/devices/bilicocoon-nest-system-bcc101) · ref BCC101 · Class IIa · EUDAMED, GUDID · status: Active
- [BiliCocoon™ Bag System](https://devicerts.com/devices/bilicocoon-bag-system-bcc201) · ref BCC201 · Class IIa · EUDAMED, GUDID · status: Active
- [BiliCocoon™ Bag Pad](https://devicerts.com/devices/bilicocoon-bag-pad-bcc211) · ref BCC211 · Class IIa · EUDAMED, GUDID · status: Active
- [BiliCocoon™ Nest Disposable](https://devicerts.com/devices/bilicocoon-nest-disposable-bcc121) · ref BCC121 · Class I · EUDAMED, GUDID · status: Active

## Source and citation

- Cite as: Neomedlight. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/neomedlight (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [FDA registration and listing](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm)
- EUDAMED record synced: 2026-11-07
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/neomedlight.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/neomedlight
- 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.