FDA.reportPublic FDA data

DIOPSYS INC.

Matched from indexed company URL: DIOPSYS, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30041744673004174467DIOPSYS INC.1N2026-01-011000 Kreider Drive STE 700 Middletown PA US 17057
30041744673004174467DIOPSYS INC.1N2020-04-2516 CHAPIN ROAD SUITE 912 PINE BROOK NJ US 07058

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
00850514007008Diopsys® - Braided ERG Lead Wire Set, Bag973-244-0622info@diopsys.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
236411365623913K101763DIOPSYS NOVA VEP VISION TESTING SYSTEMGWE2011-05-09
3426111902780782K101763DIOPSYS NOVA VEP VISION TESTING SYSTEMGWE2011-05-09
236411044692674K043491ENFANTTMGWE2005-03-16

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GWE32011-05-09

PMN#

GUDID#