Vioptix Inc

FDA Filings

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

FDA Registration(s)
Registration Number3003965364
FEI Number3003965364
NameVIOPTIX, INC.
Owner & OperatorVIOPTIX, INC.
Contact Address39655 Eureka Drive --
Newark CA 94560 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address39655 Eureka Dr
Newark, CA 94560 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
VIOPTIX, INC.
Intra.Ox Disposable Sheath OXY-2-STH-12020-04-27
VIOPTIX, INC.
Intra.Ox Optical QC Target OXY-2-QCT-12020-04-27
VIOPTIX, INC.
Intra.Ox Smart Sensor OXY-2-DUR-12020-04-27
VIOPTIX, INC.
Intra.Ox 2.0 Tissue Oximeter2019-10-23
ViOptix, Inc.
Intra.Ox 2.0 Handheld Tissue Oximeter2019-09-16
VIOPTIX, INC.
Intra.Ox Tissue Oximeter2018-10-09
VIOPTIX, INC.
T.Ox SS Sensor OXY-2-SPI-12018-07-06
VIOPTIX, INC.
T.Ox SP Sensor OXY-2-SPD-12018-07-06
VIOPTIX, INC.
Intra.Ox Handheld Tissue Oximeter2017-11-16
VIOPTIX, INC.
T.Ox Tissue Oximeter2014-10-06
VIOPTIX, INC.
Intra.Ox Handheld Tissue Oximeter2014-10-06
VIOPTIX INC.
INTRA. OX HANDHELD TISSUE OXIMETER2014-09-12
VIOPTIX, INC.
ODISSEY TISSUE OXIMETER2014-07-01
VIOPTIX, INC.
VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM2009-04-17
VIOPTIX, INC.
T.Ox Tissue Oximeter2007-10-31
VIOPTIX, INC.
ODISsey Tissue Oximeter2007-10-31
VIOPTIX, INC.
VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-22005-01-10

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