FDA.reportPublic FDA data

RADIOMED CORPORATION

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30040475283004047528RADIOMED CORPORATION1N2020-04-253150 Stage Post Drive, Suite 110 Bartlett TN US 38133

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
B8872150040X-Seed - 1.15mm x 5mm X-SEED Four Pack9014327202visicoil@izimed.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
595061519174981K161724Visicoil MR Marker (User Loaded), Visicoil MR Marker (Pre-Loaded)IYE2017-04-28
595061351782967K120859PRE-LOADED GOLD VISICOIL CK MARKERKXK2012-04-19
595061754632948K071673ONC SOLUTIONS MARKER, MODELS 001001 TO 001012 AND 001021 TO 001032IYE2007-07-18
595061747757377K070305PRE-LOADED VISICOILIYE2007-03-07
595061465216919K031206RADIOMED SOFT TISSUE MARKERJAK2003-05-21

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
IYE32017-04-28
KXK12012-04-19
JAK12003-05-21

PMN#

GENETRA

2001-12-05

RADIOMED CORPORATION

Applications#

GUDID#