FDA.report

CORINDUS, INC.

FDA Registration(s)

RegistrationFEINameStatusInitial importerExpiration yearAddress
30078225083007822508CORINDUS, INC.1N2020-04-25309 Waverley Oaks Rd Ste 105 Waltham MA US 02452

GUDID Contact Samples

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

Source GUDIDProductPhoneEmail
00816280022010CorPath 200 Control Console - 160-00043508-653-3335customer.service@corindus.com
00816280022027CorPath 200 Articulated Arm - 160-00807508-653-3335customer.service@corindus.com
00816280022034CorPath 200 Robotic Drive - 160-00050508-653-3335customer.service@corindus.com

Registered Device Listings

Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1384711317907784K180517CorPath GRX SystemDXX2018-03-29
1384711378281587K173806CorPath GRX SystemDXX2018-03-01
1384711033595199K173288CorPath GRX SystemDXX2018-02-15
1384711480903384K160121CorPath GRX SystemDXX2016-10-27
1384711155396567
1384711296481003

Product Codes Associated With Registrations

Product codeRegistration listing recordsLatest decision
DXX42018-03-29

PMN

GUDID