Fziomed Inc

FDA Filings

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

FDA Registration(s)
Registration Number2031637
FEI Number3004474407
NameFZIOMED, INC.
Owner & OperatorFZIOMED, INC.
Contact Address231 BONETTI DR. --
San Luis Obispo CA 93401 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address231 BONETTI DR
SN Luis Obisp, CA 93401 US
Establishment TypeManufacture Device in the United States for Export Only



FDA Filings

Device
Company
DeviceDate
FZIOMED, INC.
DYNAVISC2012-03-12
FZIOMED, INC.
Oxiplex2009-02-17
FZIOMED, INC.
Oxiplex/SP Gel2009-02-17
FZIOMED, INC.
Oxiplex 1mL2009-02-17
FZIOMED, INC.
MediShield2009-02-17
FZIOMED, INC.
MediShield 1mL2009-02-17
FZIOMED, INC.
Interpose2009-02-17
FZIOMED, INC.
Oxiplex/IU2009-02-17
FZIOMED, INC.
Oxiplex/AP2009-02-17

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