Nextphase Medical Devices

FDA Filings

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

FDA Registration(s)
Registration Number3007199740
FEI Number3007199740
NameNextPhase Medical Devices
Owner & OperatorNextPhase Medical Devices
Contact Address150 Hopper Ave
Waldwick NJ 07463 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address150 Hopper Ave
Waldwick, NJ 07463 US
Establishment Type
  • Manufacture Medical Device
  • Manufacture Medical Device for Another Party (Contract Manufacturer)



FDA Owner/Operator Registration


FDA Filings

Device
Company
DeviceDate
NextPhase Medical Devices
Brain injury adjunctive interpretive oculomotor assessment aid2019-02-25
NextPhase Medical Devices
Meditron Endolav EL-1002010-10-20

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