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: ILS FDA class 1

Adaptor, Hygiene

Physical Medicine

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A Hygiene Adaptor is an assistive device used in Physical Medicine and occupational therapy to enable patients with limited hand function, upper limb disability, or reduced range of motion to independently perform personal hygiene tasks such as bathing, grooming, and toileting. 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 ILS, 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

31 matches
K Number
Device Name
MEDICAL TOILET SEAT
COMMODE CHAIR 98200
RAISED TOILET SEATS & NAIL CLIPPERS
LAVATORY SEAT HEIGHTENER
TOILET SEAT RAISED
SHOWER STOOL W/HANDLES
BATHING CHAIR FOR CHILD
DISPOSABLE TOOTH BRUSH
PLASTIC BREAK RESISTANT MIRROR
LAVATORY SEAT HEIGHTENER
COLLAPSABLE LAVATORY HEIGHTENER
BK-6477 THE DERBY RAISED TOILET SEAT
HYGIENE ADAPTORS
BATHTUB GRAB BAR
CHILDS TOILET TRAINER HYGIENE AIDS
SECURA BATH SEAT
HYGIENE ADAPTORS
TUBMATE
HYGIENE ADAPTORS
GARELICK COMMODE
TOILET TRAINER FOR HANDICAPPED CHILD
ANUS STIMULATOR
SEMI-RECLINING BATH CHARI & BELT
WATER POWERED BATH CHAIR LIFT
MOTOR RISER TOLIT LIFT
TOILET AID
EXTRA LARGE LONG HANDLED SPONGE
BATHTUB RAILS
LONG HANDLED SPONGE
CONTOURED RAISED TOILET SEAT
LONG HANDLED BATH BRUSH

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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