Neomedlight
Active in EUDAMEDFrancefrom SRN EUDAMED FDA SRN FR-MF-000004044 FEI 3013919653
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.
- Devices
- 13
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
Registry facts
- Registries
- EUDAMED 10
- FDA GUDID 10
- FDA 510(k) 1
- Device classes
- EU Class I 5
- EU Class IIa 5
- FDA Class II 3
- Top EMDN categories
- Identifiers
- EUDAMED SRN FR-MF-000004044
- FDA FEI 3013919653
- DUNS 265910339
At a glance
Market reach
- European Union
- EUDAMED actor
- United States
- FDA FEI
Catalogue
Search and filter all 13 devicesCompany details
- EUDAMED SRN
- FR-MF-000004044
- FDA FEI number
- 3013919653
- DUNS number
- 265910339
- EU VAT number
- FR05800626293
- EUDAMED status
- Active
- EUDAMED registered name
- NEOMEDLIGHT
- Registered address
- 88 et 90, Frederic Fays, 69100, Villeurbanne, France
- Website
- www.neomedlight.com/fr/
- PRRC contact
- Hocine MAHAMDI
Frequently asked questions
How many devices does NEOMEDLIGHT have in the registry?
The registry currently lists 13 devices for NEOMEDLIGHT. Devices recorded under merged duplicate company entries are counted once.
Which registries list NEOMEDLIGHT's devices?
Among its 13 most recently registered devices, NEOMEDLIGHT has devices listed in EUDAMED (10 devices), FDA 510(k) (1 device) and FDA GUDID (10 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do NEOMEDLIGHT's devices fall under?
Among its 13 most recently registered devices, the classes recorded for NEOMEDLIGHT's devices are Class I, Class IIa and Class II. Each device page shows its own class and authorisation.
What are the newest devices from NEOMEDLIGHT in the registry?
The most recently registered devices listed for NEOMEDLIGHT include BiliCocoon™ Service Kit BCC010-SK10, BiliCocoon™ Bag Disposable - Small, CareMin650 ™ Oral Sleeve and Bilicocoon™ Phototherapy System.