Oculeve Inc

FDA Filings

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

FDA Registration(s)
Registration Number3013683287
FEI Number3013683287
NameOCULEVE, INC.
Owner & OperatorALLERGAN, INC.
Contact Address2525 DUPONT DRIVE --
Irvine CA 92612 US
Official Correspondent
  • David J Fisher
  • x-714-2463862-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4410 Rosewood Dr
Pleasanton, CA 94588 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
OCULEVE, INC.
TrueTear F-00572020-02-06
OCULEVE, INC.
TrueTear F-00372020-02-06
OCULEVE, INC.
TrueTear F-00592019-02-21
OCULEVE, INC.
TrueTear F-00392019-02-21
OCULEVE, INC.
TrueTear F-00502018-07-06
OCULEVE, INC.
TrueTear F-00552018-07-06
OCULEVE, INC.
TrueTear F-00562018-07-06
OCULEVE, INC.
TrueTear F-00512018-07-06
OCULEVE, INC. [ALLERGAN, INC.]
TrueTear2018-05-22
OCULEVE, INC.
TrueTear F-00302018-03-29
OCULEVE, INC.
TrueTear F-00352018-03-29
OCULEVE, INC.
TrueTear F-00362018-03-29
OCULEVE, INC.
TrueTear F-00312018-03-29
OCULEVE, INC. [ALLERGAN, INC.]
TrueTear2017-08-07
OCULEVE, INC.
Oculeve Intranasal Tear Neurostimulator Device2017-04-24

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