FDA.reportPublic FDA data

OCULEVE, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30136832873013683287OCULEVE, INC.1N2020-04-254410 Rosewood Dr Pleasanton CA US 94588

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
00850102007038TrueTear - TrueTear System+1(415)745-3784chung_susan@allergan.com
00850102007106TrueTear - TrueTear System Demo+1(415)745-3784chung_susan@allergan.com
00850102007120TrueTear - TrueTear Disposable Tip Demo+1(415)745-3784chung_susan@allergan.com
00850102007137TrueTear - TrueTear Disposable Tip+1(415)745-3784chung_susan@allergan.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2139602059755252DEN170086TrueTear Intranasal Tear NeurostimulatorQBR2018-05-17
2139601724251738DEN160030Oculeve Intranasal Tear Neurostimulator DevicePQJ2017-04-24

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
QBR12018-05-17
PQJ12017-04-24

GUDID#