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: NAE FDA class 1

Dressing, Wound, Hydrogel Without Drug And/Or Biologic

General, Plastic Surgery

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The Hydrogel Wound Dressing Without Drug or Biologic is a wound care product composed of water-based hydrogel material that provides moisture to dry wounds, facilitates autolytic debridement, and maintains a moist wound healing environment without any incorporated drug or biological agent. Classified as FDA Class 1, it is subject to general controls under regulation 878.4022 (General and Plastic Surgery specialty).

510(k) Clearances

27 matches
K Number
Device Name
MODIFICATION TO ZENIEVA
MODIFICATION TO ZENIEVA
ZENIEVA
GILTECH PLUS HYDROGEL SKIN DRESSING
DERMAPHYLYX CALCIUM ALGINATE WOUND DRESSING
AD-HEAL HYDROGEL DRESSING, VARIOUS SIZES
COMFEEL PURILON GEL,15G(3900)/COMFEEL PURILON GEL,25G(3903)
HYDROGEL SKIN DRESSING
AQUAFLO HYDROGEL WOUND DRESSING & PACKER
BIODERM MEDICAL HYDROGEL ISLAND DRESSING
CURAGEL HYDROGEL WOUND DRESSING
BRADY MEDICAL PRODUCTS TRANSCORBENT AND THINSITE TOPICAL BORDER WOUND DRESSINGS
INTRASITE
BRADY MEDICAL PRODUCTS TRANSORBENTS WOUND DRESSING
NDM HYDROGAUZE WOUND DRESSING
ALLEVYN ISLAND WOUND DRESSING
BRADY MEDICAL PRODUCTS TRANSORB WOUND DRESSING
NU-GEL ISLAND WOUND DRESSING
DUODERM HYDROCOLLOID GEL
INTRASITE GEL
CLEARSITE STERILE WOUND DRESSING, NDM WOUND DRESSI
TRANSORB(TM) ULCER & WOUND DRESSING
PROMEON HYDROGEL DRESSING #45 STERILE W/ MESH
PROMEON HYDROGEL DRESSING #45 STERILE W/O MESH
CLEARSITE HYDROGEL WOUND DRESSING MODIFICATION
DEROYAL HYDROGEL DRESSING
CLEARSITE(R) STERILE WOUND CARE 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.

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