FDA.reportPublic FDA data

ARTVENTIVE MEDICAL GROUP, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30106062213010606221ARTVENTIVE MEDICAL GROUP, INC.1N2020-04-251797 Playa Vista San Marcos CA US 92078

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
B617PG1111ArtVentive Endoluminal Occlusion System (EOS) - ArtVentive Endoluminal Occlusion System (EOS), 11mm Implant+1 (650) 465-5259customerservice@artventivemedical.com
B617PG151ArtVentive Endoluminal Occlusion System (EOS) - ArtVentive Endoluminal Occlusion System (EOS), 5mm Implant+1 (650) 465-5259customerservice@artventivemedical.com
B617PG181ArtVentive Endoluminal Occlusion System (EOS) - ArtVentive Endoluminal Occlusion System (EOS), 8mm Implant+1 (650) 465-5259customerservice@artventivemedical.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1659291787215574K150402Endoluminal Occlusion System-EOSKRD2015-09-25
1659291258422282

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KRD12015-09-25

PMN#

GUDID#