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-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K241916 | TearRepair Liquid Skin Protectant | Optmed, Inc. | 2024-09-27 | 88 | 0 |
| K182733 | Rochal Bioshield Silicone Film | Rochal Industries, LLC | 2019-06-27 | 272 | 0 |
| K171148 | Aleo BME Liquid Bandage | Aleo Bme, Inc. | 2018-01-12 | 268 | 0 |
| K153571 | Cavilon Advanced High Endurance Skin Protectant | 3M Healthcare | 2016-08-23 | 252 | 0 |
| K160684 | Atteris No-Sting Skin Protectant | Rochal Industries, LLC | 2016-07-26 | 137 | 0 |
| K131384 | KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAG | Kericure, Inc. | 2014-08-07 | 450 | 0 |
| K133443 | MARATHON NO STING LIQUID SKIN PROTECTANT | Advanced Medical Solutions (Plymouth), Ltd. | 2014-07-10 | 240 | 0 |
| K120059 | LIQUID BANDAGE | Chesson Laboratory Associates, Inc. | 2012-05-17 | 129 | 0 |
| K092712 | SKIN BARRIER FILM | Lodestar Products, Inc. | 2010-02-23 | 173 | 0 |
| K083087 | ECOCEL | Polichem S.A | 2009-08-07 | 295 | 0 |
| K083913 | CHESSON LABS LIQUID BANDAGE | Chesson Laboratory Associates, Inc. | 2009-07-31 | 213 | 0 |
| K083752 | GLUSEAL 90, MODEL GLU9010 | Glustitch, Inc. | 2009-02-23 | 68 | 0 |
| K082703 | MRDH BANDAGE | Marine Polymer Technologies, Inc. | 2008-10-14 | 28 | 0 |
| K081009 | NEUTROPHASE | Novabay Pharmaceuticals | 2008-05-20 | 42 | 0 |
| K073663 | GELSPRAY WOUND DRESSING | Biocure, Inc. | 2008-01-30 | 35 | 0 |
| K063202 | PRODERMA LIQUID BANDAGE | Procurement Technology Systems, LLC | 2007-05-02 | 194 | 0 |
| K984207 | SILVERLON DIRECT PRESSURE WOUND DRESSING | Argentum International, LLC | 2007-03-19 | 3037 | 0 |
| K062602 | BAND-AID(R) BRAND LIQUID BANDAGE | Johnson & Johnson Consumer Companies, Inc. | 2006-12-11 | 101 | 0 |
| K053409 | 3M LIQUID BANDAGE | 3M Company | 2006-06-19 | 194 | 0 |
| K042955 | CUTICOVER SKIN BARRIER DEVICE | D & D Holdings, LLC | 2006-06-19 | 601 | 0 |
| K050757 | FLEX-AID LIQUID GEL BANDAGE AND DERMAFLEX GEL TISSUE ADHESIV | Chemence Medical, Inc. | 2006-02-23 | 337 | 0 |
| K051082 | MEDTRADE PRODUCTS SKIN PROTECTIVE BARRIER WIPE (STERILE AND | Medtrade Products , Ltd. | 2005-11-08 | 195 | 0 |
| K032948 | ELASTIC SKIN LIQUID BANDAGE | Medpak, LLC | 2004-06-25 | 277 | 0 |
| K040779 | RESTORE WOUND CLEANSER | Hollister, Inc. | 2004-05-17 | 52 | 0 |
| K031321 | LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001 | Medlogic Global Limited | 2004-01-21 | 271 | 0 |
| K031263 | 3M LIQUID BANDAGE, MODEL 120-LB | 3M Company | 2003-10-07 | 169 | 0 |
| K030574 | GLUSEAL 5ML DISPENSER, 1 ML DISPENSER, .2 ML DISPENSER | Glustitch, Inc. | 2003-08-21 | 178 | 0 |
| K023163 | LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), M | Medlogic Global Limited | 2003-01-13 | 112 | 0 |
| K022645 | CURAD | Beiersdorf AG | 2002-11-05 | 89 | 0 |
| K013225 | INSTACLOT FOR OTC USE, TRAUMASSTAT FOR PRESCRIPTION USE | Medafor, Inc. | 2001-12-26 | 90 | 0 |
| K002338 | LIQUIDERM LIQUID ADHESIVE BANDAGE | Closure Medical Corp. | 2001-01-29 | 181 | 0 |
| K002550 | RDH BANDAGE | Marine Polymer Technologies, Inc. | 2000-12-20 | 125 | 0 |
| K991729 | FERRIS POLYOSTOMY STERILE WOUND DRESSING | Ferris Mfg. Corp. | 1999-08-27 | 99 | 0 |
| K992032 | ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033 | Acrymed, Inc. | 1999-08-19 | 64 | 0 |
| K991920 | DERMAPHYLYX HYDROPHILIC FOAM WOUND DRESSING | Dermaphylyx, Inc. | 1999-08-12 | 66 | 0 |
| K991933 | DERMAPHYLYX FOAM ISLAND DRESSING | Dermaphylyx, Inc. | 1999-07-30 | 52 | 0 |
| K991609 | DERMAPHYLYX SUPER ABSORBENT FIBER DRESSING | Dermaphylyx, Inc. | 1999-07-20 | 71 | 0 |
| K991608 | DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSING | Dermaphylyx, Inc. | 1999-07-20 | 71 | 0 |
| K991694 | DYNAREX DRAIN SPONGE | Dynarex Corp. | 1999-07-15 | 58 | 0 |
| K991695 | DYNAREX NON-WOVEN SPONGE | Dynarex Corp. | 1999-07-15 | 58 | 0 |
| K990955 | MODIFICATION OF:BIODERM FOAM WOUND DRESSING | Bioderm, Inc. | 1999-05-18 | 57 | 0 |
| K990906 | FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER | Ferris Mfg. Corp. | 1999-04-29 | 42 | 0 |
| K984539 | FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSING | Ferris Mfg. Corp. | 1999-03-01 | 70 | 0 |
| K973227 | ASKINA HYDROCOLLOID/THIN | B.Braun Medical, Inc. | 1999-01-28 | 519 | 0 |
| K983519 | COMFEEL SEASORB DRESSING | Coloplast Corp. | 1998-12-30 | 83 | 1 |
| K980117 | NUVO BARRIER FILM | Biomedical Development Co. | 1998-12-18 | 339 | 0 |
| K984177 | MODIFICATION TO SKVEKPATCH | Marine Polymer Technologies, Inc. | 1998-12-18 | 28 | 0 |
| K983210 | ALGISITE M | Smith & Nephew, Inc. | 1998-12-10 | 87 | 0 |
| K983833 | ACTICOAT COMPOSITE WOUND DRESSING, ACTICOAT COMPOSITE WOUND | Westaim Biomedical, Inc. | 1998-12-10 | 41 | 0 |
| K983554 | ALLDRESS, ABSORBENT FILM DRESSING | Molnlycke Health Care, Inc. | 1998-11-10 | 28 | 0 |
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