FDA.reportPublic FDA data

SYNCREON

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30118002273011800227SYNCREON1N2020-04-2519200 South Western Blvd Torrance CA US 90501

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2040591121477997K180688SLENDERTONE CoreFit Abs 8, Type 734NGX2018-10-25
2040591085531647K151903Slendertone connect AbsNGX2015-11-06
2040591666971496K100556SLENDERTONE FLEX MAX, MODEL 517 USNGX2010-08-02
2040591691690619K100320SLENDERTONE SYSTEM ULTRA MODEL E70/X70NGX2010-05-05
2040591876326865K083164SYSTEM-ARMS, MODELS 390, X60NGX2008-12-16
2040591244713305K072294SYSTEM-MINI, MODELS: 390, E30NGX2007-10-25
2040591976995320K070142SLENDERTONE SYSTEM ABS, MODELS 390, E10, X10; SLENDERTONE SYSTEM SHORTS, MODELS 390, E20NGX2007-03-23
2040591691041539K030708SLENDERTONE FLEX ABDOMINAL TRAINING SYSTEM, TYPE 515NGX2003-06-25

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NGX82018-10-25