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: ILC FDA class 1

Utensil, Eating

Physical Medicine

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Eating Utensils are adapted implements used in Physical Medicine and occupational therapy to assist patients with limited hand function, tremors, or upper limb disabilities in self-feeding, supporting independence in activities of daily living. It is classified as FDA Class 1, the lowest risk category, subject only to general controls with no premarket submission required. The product code is ILC, regulated under 21 CFR 890.5050, within the Physical Medicine medical specialty. This device is GMP exempt, indicating it is not subject to full good manufacturing practice requirements.

510(k) Clearances

32 matches
K Number
Device Name
GLOSSECTOMY FEEDING SPOONS
BATH TUB SEAT & BATH BOARD
COLLAPSABLE LAVATORY SEAT HEIGHTENER
PLASTIC BUILT-UP HANDLE EATING UTENSILS
EATING UTENSILS
BK-1129 BOTTLE STRAW
ALUMINUM SCOOP DISK
FEEDING AID KIT
EATING UTENSILS
BK-1424 INNER LIP PLATE, CERAMIC
BK-1426-00-01 STONYBROOK/HI-WALL PLATE
BK-1544 BE OK SCOOP DISK
BK-1472 SPATULA SPOON
KNIFE, LARGE HANDLE
SPORKS, PLASTIC, DISP.
UTENSILS, WEIGHTED
KNIFE, ROCKER, SLOTTED HANDLE
QUADRIPLEGIC MEAT KNIFE
BEESON AUTOMADDAK FEEDER
SQUARE FOOD GUARD
ADULT SWIVEL FORK
FOOD GUARDS
BUILT-UP HANDLE UTENSILS
PLASTIC HAND CONE
WEIGHTED FORK
WEIGHTED SPORK
CONE, HAND, BK-1501
CUP HOLDER/CUP, WHEELCHAIR
SPOON, SOFT FOOD FEEDER, BK-1473
CUP HOLDER/CUP,BK-1140
GLASS, SIP N' STRAW WITH LID, 1143
GLASS, NOSEY CUTOUT, BK-1146

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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