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: ILI FDA class 1

Sling, Arm

Physical Medicine

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An Arm Sling is an orthotic support device used in Physical Medicine to immobilize and protect the upper limb following fractures, dislocations, sprains, or surgery, holding the arm in a flexed position against the body during the healing process. 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 ILI, regulated under 21 CFR 890.3640, 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

19 matches
K Number
Device Name
MATRX, PYRAMID TRIANGLE BANDAGE
ARM SLINGS
SATO FAMILY FIRST AID KIT
VARIOUS ARM SLING
A.C. SPLINT
UNIVERSAL SLING, SLING & SWATHE
UNIVERSAL SLING, SLING & SWATHE
ORTHOPEDIC SOFT GOODS
LIMB HOLDER ARM SLING
ARM SLING, POUCH TYPE
MADDACOMFORT SLING
ARM SLINGS
BAUER & BLACK ARM SLING W/DETACH. POUCH
CONPHAR ARM SLINGS
BK-6157-02 C.V.A SLING, MEDIUM&LARGE
ARM SLING
ARM SLING
STROKE SLING
ECONOMY IMMOBILIZATION AND VELPEAN SLING

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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