Atlas FDA

Predicate Research Report · generated 2026-08-21 · Print / save as PDF · Save to account

MUI — Predicate Candidate Screening

34 FDA 510(k) clearances under this product code; the 50 most recent screened below.

121 daysmedian FDA review time
434 days90th percentile
34clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K253255Non-Sterile Ultrasound Gel Sterile Ultrasound GelFoshan Pingchuang Medical Technology Co., Ltd.2026-06-172610
K252337EdgeFlow Gel PadEdgecare, Inc.2026-04-242700
K242167Sterile and Non-Sterile Ultrasonic Coupling AgentAnhui Deepblue Medical Technology Co., Ltd.2024-09-19570
K241789Non-Sterile Ultrasound Transmission GelsHony Medical Co., Ltd.2024-07-24330
K232957Sterile and Non-Sterile Ultrasound GelsJianerkang Medical Co., Ltd.2023-12-15850
K221999Ultrasound Transmission GelsHony Medical Co., Ltd.2022-08-30540
K211691Ultrast GelUltrast, Inc.2021-12-222030
K190591Safergel Sterile Ultrasound GelSafersonic Us, Inc.2019-10-042110
K181363EcoVue Sterile and Non-Sterile Ultrasound GelsH R Pharmaceuticals, Inc.2018-06-13210
K163026Ultra/Phonic Scanning GelPharmaceutical Innovations, Inc.2018-01-094350
K163027Ultra/Phonic Free Conductivity GelPharmaceutical Innovations, Inc.2018-01-094350
K163023Other-Sonic Transmission GelPharmaceutical Innovations, Inc.2018-01-084340
K163024Ultra/Phonic Conductivity GelPharmaceutical Innovations, Inc.2018-01-084340
K163050Advance Medical Designs, Inc. Sterile Ultrasound GelAdvance Medical Designs, Inc.2017-10-253580
K151070Sonishield 100 Antimicrobial Ultrasound GelQuotient Medical2016-01-132670
K130581KONIX STERILE GELTurkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa2014-06-184704
K131905SOLID GEL PADBluemtech2013-07-18220
K130041SHEATHES STERILE ULTRASOUND GELSheathing Technologies, Inc.2013-02-06290
K121311THIXO-GEL ULTRASOUND SPRAYCloverline International Pharma Services GmbH2012-08-301210
K112827SHEATHES ULTRASOND GELSheathing Technologies, Inc.2012-06-222680
K102637DYNAREX ULTRASOUND GELDynarex Corporation2011-02-161550
K102683THE ADDITIONOb The-Addition, LLC2011-01-061110
K083358LUBRICANO-ULTRASOUNDFarco Pharma GmbH2009-01-09870
K072515EMBRACE GELOrison Corporation2007-09-20130
K042619ULTRABIO - IN VIVO BIOCOMPATIBLE, BIOELIMINATED STERILE ULTRSonotech, Inc.2004-11-05420
K033178ULTRABIOSonotech, Inc.2004-08-043080
K031018AUTOGEL PADRich-Mar Corp.2003-12-082520
K031222SCANLUBESonotech, Inc.2003-07-23970
K031894SCANTEC PADSonotech, Inc.2003-07-18290
K030889ULTRAEKOGEL MODELS EK 2000 & EK 2001Inmed Ltda.2003-05-23630
K020956VIVOSONIC DIANOSTIC ULTRASOUND IMAGING COUPLING MEDIAMicrotek Medical, Inc.2002-05-16520
K021132UNI-PATCH ULTRASOUND COUPLING GELThe Ludlow Company LP2002-05-15360
K013212WAVELENGHT ULTRASOUND LOTIONNational Therapy Products, Inc.2002-02-251530
K827296POLYSONIC ULTRASOUND LOTIONParker Laboratories, Inc.1982-04-16170

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda