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.
Registration Number | 3003965364 |
FEI Number | 3003965364 |
Name | VIOPTIX, INC. |
Owner & Operator | VIOPTIX, INC. |
Contact Address | 39655 Eureka Drive -- Newark CA 94560 US |
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 39655 Eureka Dr Newark, CA 94560 US |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
VIOPTIX, INC. | Intra.Ox Disposable Sheath OXY-2-STH-1 | 2020-04-27 |
VIOPTIX, INC. | Intra.Ox Optical QC Target OXY-2-QCT-1 | 2020-04-27 |
VIOPTIX, INC. | Intra.Ox Smart Sensor OXY-2-DUR-1 | 2020-04-27 |
VIOPTIX, INC. | Intra.Ox 2.0 Tissue Oximeter | 2019-10-23 |
ViOptix, Inc. | Intra.Ox 2.0 Handheld Tissue Oximeter | 2019-09-16 |
VIOPTIX, INC. | Intra.Ox Tissue Oximeter | 2018-10-09 |
VIOPTIX, INC. | T.Ox SS Sensor OXY-2-SPI-1 | 2018-07-06 |
VIOPTIX, INC. | T.Ox SP Sensor OXY-2-SPD-1 | 2018-07-06 |
VIOPTIX, INC. | Intra.Ox Handheld Tissue Oximeter | 2017-11-16 |
VIOPTIX, INC. | T.Ox Tissue Oximeter | 2014-10-06 |
VIOPTIX, INC. | Intra.Ox Handheld Tissue Oximeter | 2014-10-06 |
VIOPTIX INC. | INTRA. OX HANDHELD TISSUE OXIMETER | 2014-09-12 |
VIOPTIX, INC. | ODISSEY TISSUE OXIMETER | 2014-07-01 |
VIOPTIX, INC. | VESSELINK MICROVASCULAR ANASTOMOTIC COUPLER SYSTEM | 2009-04-17 |
VIOPTIX, INC. | T.Ox Tissue Oximeter | 2007-10-31 |
VIOPTIX, INC. | ODISsey Tissue Oximeter | 2007-10-31 |
VIOPTIX, INC. | VIOPTIX ODISSEY TISSUE OXIMETER TISSUE OXIMETER, MODEL OXY-2 | 2005-01-10 |
NCAGE Code | 4CC62 | VIOPTIX, INC. |
CAGE Code | 4CC62 | VIOPTIX, INC. |
S.A.M. Registration | 4CC62 [127211923] | VIOPTIX, INC. |
SEC | 0001106646 | VIOPTIX INC of DELAWARE |