Nichrominox

FDA Filings

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

FDA Registration(s)
Registration Number3008519369
FEI Number3008519369
NameNICHROMINOX
Owner & OperatorNICHROMINOX
Contact Address18 RUE DES FRERES LUMIERE
SAINT BONNET DE MURE FR-69 Rhone 69720 FR
Official Correspondent
  • ERIC LEFRANCQ-LUMIERE
  • 033-478-740415-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address18 RUE DES FRERES LUMIERE
SAINT BONNET DE MURE Rhone, 69720 FR
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Develop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
NICHROMINOX
 W&H PS5022032025-12-30
NICHROMINOX
 W&H PS5022042025-12-30
NICHROMINOX
 W&H PS5015982025-12-30
NICHROMINOX
Empty Organizer2019-01-22
NICHROMINOX
IntraSpin Xpression Box2013-05-16

Related Finance Registrations
NCAGE CodeF1884NICHROMINOX
CAGE CodeF1884NICHROMINOX
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