FDA.reportPublic FDA data

InNeuroCo, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30122410933012241093InNeuroCo, Inc.1N2020-04-254635 NW 103RD AVE Sunrise FL US 33351
30141747163014174716InNeuroCo1N2020-04-2511611 Interchange Circle South Miramar FL US 33025

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
00816900020013Intermediate Catheter - Intermediate Catheter, Hemostasis Valve, & Introducer(954) 742-5988Complaints@InNeuroCo.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1892801333441646K181354074 Zenith Flex SystemNRY2018-10-25
2147001333441646K181354074 Zenith Flex SystemNRY2018-10-25
1892801234606192K172468091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cmDQY2017-12-06
2147001234606192K172468091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cmDQY2017-12-06
1892801866388605K172167Zenith Flex SystemNRY2018-04-19
2147001866388605K172167Zenith Flex SystemNRY2018-04-19
1892801169221382K161262Super Distal Access (SDA)DQY2016-09-19
1892801862888692K152202Intermediate Catheter, 105 cm, Intermediate Catheter, 115cm, Intermediate Catheter , 125cmDQY2015-12-14
2147001699425407

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NRY42018-10-25
DQY42017-12-06

PMN#

GUDID#