FDA.reportPublic FDA data

anax USA

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30094321603009432160anax USA1Y2026-01-01406 I ST NW ARDMORE Ardmore OK US 73401

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1385521596371486K981091NEOCOLLOID, ORTHOPRINTELW1998-05-21
1385521356728202K2437203Delta UNlimitedEBF2024-12-18
1385521024914070K192251Livento Press, Soprano 10, SopranoEIH2020-01-15
1385521441029165K173908DESS Dental Smart SolutionsNHA2018-06-15
1385521128414366K170588DESS Dental Smart SolutionsNHA2017-08-08
1385521694429441K150432IDODENTINE DISC, IDODENTINE BLOCKEBG2015-08-14
1385521385860745K132937HARVEST DENTAL POLYMER BLOCKS (ZCAD, AURORA)EBG2014-05-21
1385521620269010K123638PEKKTON IVORYEBG2013-02-21
1385522067156607K112044ANAXBLEND MODEL 20XXX (SEVERAL), ANAXGUM MODEL 25XXX (U), MOCK-UP DIRECT MODEL 240XXX (U), MOCK-UP DIRECT FLOW MODEL 24AEBF2012-01-26
1385521842787158K052073FUTURAPRESS LT, N AND HP, FUTURAJET, FUTURASELF, FUTURAGEN AND FUTURACRYL 2000EBI2005-10-26
1385521513069767K023079NEW OUTLINEEBG2002-10-30
1385521818794491

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
EBG42015-08-14
EBF22024-12-18
NHA22018-06-15
EIH12020-01-15
EBI12005-10-26
ELW11998-05-21