FDA.reportPublic FDA data

INTERVENE INC

Matched from indexed company URL: Intervene, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30304811183030481118INTERVENE INC1N2026-01-012684 Middlefield Rd Ste E Redwood City CA US 94063

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
00860008103826Recana Collection Basket, 18mm - FG0156509957137customerservice@intervene-med.com
00860008103833Recana Collection Basket, 30mm - FG0166509957137customerservice@intervene-med.com
00860008103840Recana Introducer Sheath, 13Fr x 30cm - FG0176509957137customerservice@intervene-med.com
00860008103857Recana Introducer Sheath, 13Fr x 90cm - FG0186509957137customerservice@intervene-med.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3441881593023701K251185Recana Thrombectomy Catheter System (FG014. FG015, FG016, FG017, FG018, FG019, FG020)QEW2025-10-22

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
QEW12025-10-22

PMN#

GUDID#

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