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: IQI FDA class 1

Orthosis, Limb Brace

Physical Medicine

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A limb brace orthosis is an external support device applied to a limb to stabilize joints, correct alignment, or limit motion following injury, surgery, or in the management of neuromuscular conditions. It is classified as FDA Class 1, the lowest risk category, subject only to general controls. The product code is IQI, regulated under 21 CFR 890.3475, within the Physical Medicine medical specialty. This device is GMP exempt.

510(k) Clearances

50+ matches
K Number
Device Name
Neurosplint
SENSOR WALK
SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1
ACCUFLEX DYNAMIC ELBOW ORTHOSIS
MCCONNELL SHOULDER BRACE
GAIT-AID ORTHOPEDIC INSOLE
ADJUSTABLE POLYCENTRIC ELBOW HINGE
DROP FOOT BRACE
VARIOUS SUPPORTS AND SPLINTS
BRACE-UP ALL PURPOSE WRIST BAND
ROTATION BOOT
BRACE-UP STOCKING KNEE BRACE
UNIVERSAL DYNASPLINT
SPORT SUPPORTS
FRACTURE BRACING
ORTHOTIC FABRICATION ACCESSORIES
OBTHOSES
WARM'N FORM SPORTS SUPPORTS
WARM & FORM KNEE SUPPORTS
MULTITUBULAR AIR SPLINT KIT
ANKLE-FOOT CAST/SPLINT
ORTHO-FRAC KIT
FOREARM & KNEE STRAPS
HUMERAL FRACTURE CAST BRACE
PRO COMFORT TENNIS ELBOW SUPPORT/WRIST
LIMB ORTHOSIS
AIRCAST TENNIS ARM BAND
PLASTIC FRACTURE CAST BRACE KNEE JOINT
HUMERAL FRACTURE BRACE
ULNAR FRACTURE BRACE
TIBIAL FRACTURE BRACE
C-SPLINT
HUMEROUS FRACTURE BRACE, ULNA FRACTURE
BAUER & BLACK RIGID WRIST BRACE
BK-1520-01 ECONOMY WRIST SUPPORT, CHILD
OHC DYNAMIC CLUB FOOT BRACE
PARAPODIUM
SECUTEX KNEE BAND
SECUTEX WRIST BRACE
SECUTEX ANKLE BAND
SECUTE ELBOW BAND
CAST BRACE COMPONENTS
FOOT POSITIONER
AIRSTIRRUP PNEUMATIC ANKLE BRACE
ORTHOSISES DEVICES
BRACE, TENNIS ELBOW
FOOT DROP BOOT
SPLINT, BOHLER
KNEE SEPARATOR
ORTHOTIC BRACING

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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