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.
 Oxiplex 2025-09-19
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

Related Finance Registrations
NCAGE Code4CSF8FZIOMED, INC
CAGE Code4CSF8FZIOMED, INC
DUNS966718371FZIOMED, INC
SEC0001075779FZIOMED INC of CALIFORNIA
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.