Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

KMJ — Predicate Candidate Screening

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

86 daysmedian FDA review time
222 days90th percentile
49clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K142473Lubricating JellySion Biotext Medical , Ltd.2015-04-132220
K141028COLONGLIDE LUBRICANTPediatric Pharmaceuticals, Inc.2014-07-24930
K131617COLONGLIDE(R) LUBRICANTPediatric Pharmaceuticals, Inc.2013-10-031220
K121390LUBE JELLY SURINGENurse Assist, Inc.2012-08-10930
K113689DUKAL LUBRICATING JELLYDukal Corporation2012-05-041410
K112110STERILE LUBRICATING JELLYJianerkang Medical Dressing Company2012-04-102630
K103718DYNACOR LUBRICATION GELMedline Industries, Inc.2011-05-101400
K101522ULTRA SEAL STERILE LUBRICATING JELLYUltra Seal Corporation2010-12-232040
K092488DYNAREX STERILE LUBRICATING JELLYDynarex Corporation2009-12-181271
K083189STERI-LUB LUBRICATION GELAvail Medical Products, Inc.2008-11-21230
K073684SHEFFIELD PHARMACEUTICALS (STERILE) LUBRIGELSheffield Industries, Div. of Faria , Ltd.2008-05-221461
K080042SPIRUS MEDICAL SURGICAL INSTRUMENTSpirus Medical, Inc.2008-04-03860
K042563DUREX PLAY WARMER LUBRICANTSsl Americas, Inc.2005-02-231550
K041060E-Z LUBRICATING JELLYChester Labs, Inc.2004-05-07140
K020586GOOD LUBRICATIONSBiofilm, Inc.2003-01-243360
K974768PDI STERILE LUBRICATING JELLYNice-Pak Products, Inc.1998-01-16250
K973557LUBRIGLIDEQualis, Inc.1997-10-10210
K961502LUBRICATING JELLY, LOW VISCOSITYSpan-America Medical Systems, Inc.1996-07-18900
K961222EVRON GELPharmaceutical Innovations, Inc.1996-06-26900
K951431AQUAGEL LUBRICATING JELLYDepuy Healthcare1995-07-211160
K943010MAXILUBEMission Pharmacal Co.1995-07-193900
K944969STERI-LUB LUBRICATION GELHorizon Medical, Inc.1995-02-271390
K935299ASTROGLIDEBiofilm, Inc.1994-02-181080
K915574COMFORT PERSONAL LUBRICANTHyman, Phelps & McNamara, P.C.1993-02-194350
K912975OPERAND LUBRICATING JELLYGeneral Medical Co.1991-09-27810
K910790MENTOR LUBRICATING JELLYMentor Corp.1991-05-03670
K903910LUBRICATING JELLYLake Pharmaceutical, Inc.1990-10-26640
K903717DISPENSA-LUBEGam-Med Packaging Corp.1990-09-06230
K900110OPERAND* LUBRICATING JELLYGeneral Medical Co.1990-05-021130
K895406OSBON PERSONAL LUBRICANTOsbon Medical Systems, Ltd.1989-12-01860
K896207OSBON PERSONAL LUBRICANTOsbon Medical Systems, Ltd.1989-12-01360
K882506MODIFIED AMERICAN LUBRICATING JELLY, 2.7 & 5.0Span-America Medical Systems, Inc.1988-09-09920
K881338CONDOM-MATE VAGINAL LUBRICANTUpsher-Smith Laboratories, Inc.1988-05-16480
K872128K-GELTaro Pharmaceuticals, Inc.1987-06-12100
K870742AMERICAN LUBRICATING JELLY STERILE 2.7G & 5GSpan-America Medical Systems, Inc.1987-06-051000
K871169LUBRICATING JELLYH & P Industries, Inc.1987-04-0182
K864556AQUALUBE(TM)Parker Laboratories, Inc.1986-12-01120
K854155STERILE SALINE SOLUTIONI M, Inc.1985-12-10600
K853653SANA-LUBEHuntington Laboratories, Inc.1985-11-13710
K851617TODAY PERSONAL LUBRICANTVli Corp.1985-06-06490
K822143TOMAC LUBRICATING JELLYAmerican Medical Systems, Inc.1982-07-3090
K820587WET PACK LINE OF PRODUCTSAbco Dealers, Inc.1982-03-26220
K812297A.D.T. PROCEDURES TRAYA.D.T. Lab Industries1981-09-28450
K810310K-Y LUBRICATING JELLYJohnson & Johnson Professionals, Inc.1981-04-21750
K810049PEDICAT*Pollak (Intl.), Ltd.1981-04-21980
K791970HYGENIC RUBBER DAM LUBRICANTThe Hygenic Corp.1979-11-16450
K791243LUBRICATING JELLYAbco Dealers, Inc.1979-08-03250
K790087LUBRICANT, OTRHO PERSONALOrtho Pharmaceutical Corp.1979-02-01150
K770498PRESERVE LUBRICANT CODE NO. 43=4035Codman & Shurtleff, Inc.1977-06-20980

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