Randy Russell

FDA Filings

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

FDA Registration(s)
Registration Number9710154
FEI Number3003347293
NameRandy Russell
Owner & OperatorQ-MED AB
Contact AddressSEMINARIEGATAN 21 --
UPPSALA SE-C Uppsala lan [SE-03] SE-752 28 SE
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address14501 North Freeway
Fort Worth, TX 76177 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Randy Russell [Q-MED AB]
Durolane2017-09-25
Randy Russell [Q-MED AB]
Restylane Refyne2017-02-21
Randy Russell [Q-MED AB]
Restylane Defyne2017-02-21
Randy Russell [Q-MED AB]
Solesta2011-10-17
Randy Russell [Q-MED AB]
Restylane2007-12-13
Randy Russell [Q-MED AB]
Restylane-L2007-12-13
Randy Russell [Q-MED AB]
Restylane Silk2007-12-13
Randy Russell [Q-MED AB]
Perlane2007-12-13
Randy Russell [Q-MED AB]
Perlane-L2007-12-13
Randy Russell [Q-MED AB]
Restylane2007-12-13
Randy Russell [Q-MED AB]
Restylane-L2007-12-13
Randy Russell [Q-MED AB]
Restylane Silk2007-12-13
Randy Russell [Q-MED AB]
Perlane2007-12-13
Randy Russell [Q-MED AB]
Perlane-L2007-12-13
Randy Russell [Q-MED AB]
Deflux metal needle2007-10-31
Randy Russell [Q-MED AB]
Deflux injectable gel2007-10-31

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