FDA.reportPublic FDA data

CROSPON LTD.

Matched from indexed company URL: Crospon Ltd.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30068977783006897778CROSPON LTD.1N2020-04-25Galway Business Park Dangan Galway Galway IE 00000

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
05391530810029EndoFLIP - EndoFLIP Measurement Catheter for use with EndoFLIP System8552767766info@crospon.com
05391530810159EsoFLIP - EsoFLIP Dilation Catheter for use with EndoFLIP System8552767766info@crospon.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
819581040148994K183072EndoFLIP SystemFFX2019-02-15
819581519658526K172128EsoFLIP® ES-310 Balloon CatheterPIE2017-11-22
819581180631802K142000ESOFLIP ESPIE2014-09-25
819581822749821K132337ESOFLIP BALLOON DILATION CATHETERPID2013-10-07

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PIE22017-11-22
FFX12019-02-15
PID12013-10-07

PMN#

GUDID#