FDA.reportPublic FDA data

THE REFLUX COMPANY

Matched from indexed company URL: The Reflux Company

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30391676373039167637THE REFLUX COMPANY1N2026-01-017868 Silverton Ave Ste J San Diego CA US 92126

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
00856219002102Mederi MDRF1 Generator - Mederi MDRF1 Generator Monopolar generator to be used only with Secca and Stretta catheters2039309980mlucey@mederi-inc.com
00856219002102Mederi MDRF1 Generator - Mederi MDRF1 Generator Monopolar generator to be used only with Secca and Stretta catheters858-397-2200contact@refluxcompany.com
00856219002294Stretta - Stretta Catheter and Accessory Kit for use only with Mederi MDRF1 Generator2039309980mlucey@mederi-inc.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3411901569082513K173934Reza Band, Reflux BandPKA2018-04-13
3411901876304186K152317Stretta CatheterGEI2015-09-23
3411901841905386K014216SECCA SYSTEMGEI2002-03-21
3411901011196009
3411901543474534

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEI22015-09-23
PKA12018-04-13

GUDID#