Atlas FDA

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

KMF — Predicate Candidate Screening

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

79 daysmedian FDA review time
272 days90th percentile
222clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K241916TearRepair Liquid Skin ProtectantOptmed, Inc.2024-09-27880
K182733Rochal Bioshield Silicone FilmRochal Industries, LLC2019-06-272720
K171148Aleo BME Liquid BandageAleo Bme, Inc.2018-01-122680
K153571Cavilon Advanced High Endurance Skin Protectant3M Healthcare2016-08-232520
K160684Atteris No-Sting Skin ProtectantRochal Industries, LLC2016-07-261370
K131384KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGKericure, Inc.2014-08-074500
K133443MARATHON NO STING LIQUID SKIN PROTECTANTAdvanced Medical Solutions (Plymouth), Ltd.2014-07-102400
K120059LIQUID BANDAGEChesson Laboratory Associates, Inc.2012-05-171290
K092712SKIN BARRIER FILMLodestar Products, Inc.2010-02-231730
K083087ECOCELPolichem S.A2009-08-072950
K083913CHESSON LABS LIQUID BANDAGEChesson Laboratory Associates, Inc.2009-07-312130
K083752GLUSEAL 90, MODEL GLU9010Glustitch, Inc.2009-02-23680
K082703MRDH BANDAGEMarine Polymer Technologies, Inc.2008-10-14280
K081009NEUTROPHASENovabay Pharmaceuticals2008-05-20420
K073663GELSPRAY WOUND DRESSINGBiocure, Inc.2008-01-30350
K063202PRODERMA LIQUID BANDAGEProcurement Technology Systems, LLC2007-05-021940
K984207SILVERLON DIRECT PRESSURE WOUND DRESSINGArgentum International, LLC2007-03-1930370
K062602BAND-AID(R) BRAND LIQUID BANDAGEJohnson & Johnson Consumer Companies, Inc.2006-12-111010
K0534093M LIQUID BANDAGE3M Company2006-06-191940
K042955CUTICOVER SKIN BARRIER DEVICED & D Holdings, LLC2006-06-196010
K050757FLEX-AID LIQUID GEL BANDAGE AND DERMAFLEX GEL TISSUE ADHESIVChemence Medical, Inc.2006-02-233370
K051082MEDTRADE PRODUCTS SKIN PROTECTIVE BARRIER WIPE (STERILE AND Medtrade Products , Ltd.2005-11-081950
K032948ELASTIC SKIN LIQUID BANDAGEMedpak, LLC2004-06-252770
K040779RESTORE WOUND CLEANSERHollister, Inc.2004-05-17520
K031321LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001Medlogic Global Limited2004-01-212710
K0312633M LIQUID BANDAGE, MODEL 120-LB3M Company2003-10-071690
K030574GLUSEAL 5ML DISPENSER, 1 ML DISPENSER, .2 ML DISPENSERGlustitch, Inc.2003-08-211780
K023163LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MMedlogic Global Limited2003-01-131120
K022645CURADBeiersdorf AG2002-11-05890
K013225INSTACLOT FOR OTC USE, TRAUMASSTAT FOR PRESCRIPTION USEMedafor, Inc.2001-12-26900
K002338LIQUIDERM LIQUID ADHESIVE BANDAGEClosure Medical Corp.2001-01-291810
K002550RDH BANDAGEMarine Polymer Technologies, Inc.2000-12-201250
K991729FERRIS POLYOSTOMY STERILE WOUND DRESSINGFerris Mfg. Corp.1999-08-27990
K992032ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033Acrymed, Inc.1999-08-19640
K991920DERMAPHYLYX HYDROPHILIC FOAM WOUND DRESSINGDermaphylyx, Inc.1999-08-12660
K991933DERMAPHYLYX FOAM ISLAND DRESSINGDermaphylyx, Inc.1999-07-30520
K991609DERMAPHYLYX SUPER ABSORBENT FIBER DRESSINGDermaphylyx, Inc.1999-07-20710
K991608DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSINGDermaphylyx, Inc.1999-07-20710
K991694DYNAREX DRAIN SPONGEDynarex Corp.1999-07-15580
K991695DYNAREX NON-WOVEN SPONGEDynarex Corp.1999-07-15580
K990955MODIFICATION OF:BIODERM FOAM WOUND DRESSINGBioderm, Inc.1999-05-18570
K990906FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLERFerris Mfg. Corp.1999-04-29420
K984539FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSINGFerris Mfg. Corp.1999-03-01700
K973227ASKINA HYDROCOLLOID/THINB.Braun Medical, Inc.1999-01-285190
K983519COMFEEL SEASORB DRESSINGColoplast Corp.1998-12-30831
K980117NUVO BARRIER FILMBiomedical Development Co.1998-12-183390
K984177MODIFICATION TO SKVEKPATCHMarine Polymer Technologies, Inc.1998-12-18280
K983210ALGISITE MSmith & Nephew, Inc.1998-12-10870
K983833ACTICOAT COMPOSITE WOUND DRESSING, ACTICOAT COMPOSITE WOUND Westaim Biomedical, Inc.1998-12-10410
K983554ALLDRESS, ABSORBENT FILM DRESSINGMolnlycke Health Care, Inc.1998-11-10280

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