FDA.reportPublic FDA data

IMACOR, Inc

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30063821853006382185IMACOR, Inc1N2026-01-0150 Jericho Turnpike Suite 105 Jericho NY US 11753

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
00086158900201ImaCor Inc. - Ultrasound Machine for use with ClariTEE probe6312557183rlanzillotto@dukal.com
00861589000108ClariTEE - TEE ultrasound probe, single use, EO Sterile516 393 0970jkujawski@Imacorinc.com
00861589000115ImaCor Inc. - Ultrasound Machine for use with ClariTEE probe6312557183rlanzillotto@dukal.com
00861589000207ImaCor Inc. - Ultrasound Machine for use with ClariTEE probe6312557183rlanzillotto@dukal.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
900541495441336K220490ImaCor Zura Handheld ZHH-010IYN2022-04-08
900541729163480K142054IMACOR ZURA EVO IMAGING SYSTEMIYO2014-09-29
900541895340190K100989ZURA TEE SYSTEM WITH CLARITEE PROBEIYN2010-06-25
900541301710086K080223ZURA TEE SYSTEMIYO2008-06-24

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
IYN22022-04-08
IYO22014-09-29

PMN#

GUDID#