Diopsys Inc

FDA Filings

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

FDA Registration(s)
Registration Number3004174467
FEI Number3004174467
NameDIOPSYS INC.
Owner & OperatorDIOPSYS INC.
Contact Address16 CHAPIN ROAD SUITE 912 --
Pine Brook NJ 07058 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address16 CHAPIN ROAD SUITE 912
PINE BROOK, NJ 07058 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS, INC.
Diopsys® 2018-07-06
DIOPSYS INC.
Diopsys Retina Plus2011-10-06
DIOPSYS INC.
Diopsys NOVA2011-10-06
DIOPSYS INC.
Diopsys NOVA ARGOS2011-10-06
DIOPSYS INC.
DIOPSYS NOVA VEP VISION TESTING SYSTEM2011-05-09
DIOPSYS INC.
Enfant2008-01-16
DIOPSYS INC.
ENFANTTM2005-03-16

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