Neomedlight

FDA Filings

This page includes the latest FDA filings for Neomedlight. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3013919653
FEI Number3013919653
NameNEOMEDLIGHT
Owner & OperatorNEOMEDLIGHT
Contact AddressPARC EMMANUELLE LENNE 88 RUE FREDERIC FA
VILLEURBANNE FR-V Rhone-Alpes 69100 FR
Official Correspondent
  • PIERRE N saint girons
  • 33-6-33902900-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressPARC EMMANUELLE LENNE 88 RUE FREDERIC FAYS
VILLEURBANNE Rhone-Alpes, 69100 FR
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
NEOMEDLIGHT
BiliCocoon™ Service Kit BCC010-SK102024-02-16
NEOMEDLIGHT
BiliCocoon™ Fixation System BCC3012024-02-16
NEOMEDLIGHT
BiliCocoon™ Bag Pad BCC2112024-02-16
NEOMEDLIGHT
BiliCocoon™ Bag System BCC2012024-02-16
NEOMEDLIGHT
BiliCocoon™ Nest Pad BCC1112024-02-16
NEOMEDLIGHT
BiliCocoon™ Nest System BCC1012024-02-16
NEOMEDLIGHT
BiliCocoon™ Light Box BCC0102024-02-16
NEOMEDLIGHT
BiliCocoon Service Kit (x10)2017-10-10
NEOMEDLIGHT
BiliCocoon Nest System2017-10-10
NEOMEDLIGHT
BiliCocoon Nest Pad2017-10-10
NEOMEDLIGHT
BiliCocoon Nest Disposable2017-10-10
NEOMEDLIGHT
BiliCocoon Nest Disposable (x50)2017-10-10
NEOMEDLIGHT
BiliCocoon Light Box2017-10-10
NEOMEDLIGHT
BiliCocoon Fixation System2017-10-10
NEOMEDLIGHT
BiliCocoon Bag System2017-10-10
NEOMEDLIGHT
BiliCocoon Bag Pad2017-10-10
NEOMEDLIGHT
BiliCocoon Bag Disposable2017-10-10
NEOMEDLIGHT
BiliCocoon Bag Disposable (x50)2017-10-10
NEOMEDLIGHT
Bilicocoon™ Phototherapy System2017-10-06

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