NEOMEDLIGHT

FDA Device Registration & Listing · VILLEURBANNE Auvergne-Rhone-Alpes, FR · Registration 3013919653

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013919653
FEI Number
3013919653
Entity Name
NEOMEDLIGHT
City/State/Country
VILLEURBANNE Auvergne-Rhone-Alpes, FR
Establishment Address
PARC EMMANUELLE LENNE 88 RUE FREDERIC FAYS, VILLEURBANNE Auvergne-Rhone-Alpes 69100, FR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NEOMEDLIGHT (Owner Number: 10054514)
Owner / Operator Contact Address
PARC EMMANUELLE LENNE 88 RUE FREDERIC FAYS, VILLEURBANNE, FR-ARA 69100, FR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

BiliCocoon

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LBI Unit, Neonatal Phototherapy General Hospital Class 2 880.5700 2017-10-10

Official Correspondent

Cedric Brochier

US Agent Details

Gabriel MAILLOT Business: ORCOMUS Email: gmaillot@orcomus.com Phone: (415) 6455140

Related Public Records

Same Entity

NEOMEDLIGHT
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013919653. Last updated year: 2026. Please use registration number 3013919653 when referencing this establishment in official correspondence.
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