Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: KMF FDA class 1

Bandage, Liquid

General Hospital

View full classification →

A Liquid Bandage is a topical wound care product applied as a liquid or spray that forms a thin, flexible, water-resistant film over minor cuts, abrasions, and skin irritations to protect the wound from contamination and promote healing. It is classified as FDA Class 1, indicating low risk subject to general controls with no premarket approval required. The product code is KMF and the applicable regulation is 21 CFR 880.5090 in the General Hospital specialty. This device is eligible for third-party review.

510(k) Clearances

50+ matches
K Number
Device Name
TearRepair Liquid Skin Protectant
Rochal Bioshield Silicone Film
Aleo BME Liquid Bandage
Cavilon Advanced High Endurance Skin Protectant
Atteris No-Sting Skin Protectant
KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGE
MARATHON NO STING LIQUID SKIN PROTECTANT
LIQUID BANDAGE
SKIN BARRIER FILM
ECOCEL
CHESSON LABS LIQUID BANDAGE
GLUSEAL 90, MODEL GLU9010
MRDH BANDAGE
NEUTROPHASE
GELSPRAY WOUND DRESSING
PRODERMA LIQUID BANDAGE
SILVERLON DIRECT PRESSURE WOUND DRESSING
BAND-AID(R) BRAND LIQUID BANDAGE
3M LIQUID BANDAGE
CUTICOVER SKIN BARRIER DEVICE
FLEX-AID LIQUID GEL BANDAGE AND DERMAFLEX GEL TISSUE ADHESIVE PROFESSIONAL LIQUID BANDAGE
MEDTRADE PRODUCTS SKIN PROTECTIVE BARRIER WIPE (STERILE AND PRESERVED)
ELASTIC SKIN LIQUID BANDAGE
RESTORE WOUND CLEANSER
LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001
3M LIQUID BANDAGE, MODEL 120-LB
GLUSEAL 5ML DISPENSER, 1 ML DISPENSER, .2 ML DISPENSER
LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020
CURAD
INSTACLOT FOR OTC USE, TRAUMASSTAT FOR PRESCRIPTION USE
LIQUIDERM LIQUID ADHESIVE BANDAGE
RDH BANDAGE
FERRIS POLYOSTOMY STERILE WOUND DRESSING
ACRY ISLAND BORDER DRESSING, MODELS 2031, 2032, 2033
DERMAPHYLYX HYDROPHILIC FOAM WOUND DRESSING
DERMAPHYLYX FOAM ISLAND DRESSING
DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSING
DERMAPHYLYX SUPER ABSORBENT FIBER DRESSING
DYNAREX DRAIN SPONGE
DYNAREX NON-WOVEN SPONGE
MODIFICATION OF:BIODERM FOAM WOUND DRESSING
FERRIS POLYMEM POLYWIC STERILE CAVITY WOUND FILLER
FERRIS POLYMEM CALCIUM ALGINATE STERILE WOUND DRESSING
ASKINA HYDROCOLLOID/THIN
COMFEEL SEASORB DRESSING
MODIFICATION TO SKVEKPATCH
NUVO BARRIER FILM
ACTICOAT COMPOSITE WOUND DRESSING, ACTICOAT COMPOSITE WOUND DRESSING-ADHESIVE
ALGISITE M
ALLDRESS, ABSORBENT FILM DRESSING

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

Popular Product Codes

Commonly searched