FDA.reportPublic FDA data

QXMEDICAL, LLC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30097663153009766315QXMEDICAL, LLC1N2026-01-012820 Patton Rd Saint Paul MN US 55113

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
00853892004003Q50 Plus - Q50 Plus Stent Graft Balloon Catheter, 65cm877-306-5656admin@qxmedical.com
00853892004010Q50 Plus - Q50 Plus Stent Graft Balloon Catheter, 100cm651-842-2050admin@qxmedical.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1441831214057550K183679Occlusion Balloon CatheterMJN2019-04-24
1441831751674362K160561Boosting CatheterDQY2016-11-02
1441831369934665K120381Q50 PLUS STENT GRAFT BALLOON CATHETERDQY2012-02-24
1441831053562142
1441831373531793
1441831413067660
1441831714428951
1441831788600794
1441831897798930
1441831947110232

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
DQY22016-11-02
MJN12019-04-24

PMN#

GUDID#