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: LBB FDA class 2

Dynamometer, Ac-Powered

Orthopedic

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An AC-powered dynamometer is a powered instrument used in orthopedic and physical medicine settings to measure muscular strength, endurance, and joint torque during clinical assessment or rehabilitation. It is classified as FDA Class 2, indicating moderate risk and the requirement for 510(k) premarket clearance to demonstrate substantial equivalence to a predicate device. The product code is LBB, regulated under 21 CFR 888.1240, in the Orthopedic specialty. No special risk flags apply.

510(k) Clearances

36 matches
K Number
Device Name
Hoggan Scientific® microFET2™
FACTS HAND AND PINCH GRIP COMBO
DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH5006
DYNAMOMETER - MODEL FCE AND MODEL MSC
KADANCE 2000
DIGIT-GRIP WITH LCD, MODEL NUMBER DGR 002
ORO-FACIAL MYOGRAPHIC MEASUREMENT INSTRUMENT (OMMI)
MEKANIKA'S SPINAL STIFFNESS GAUGE (SSG)
DYNAMOMETER
GREENLEAF EVAL SYSTEM/ GREENLEAF SOLOSYSTEM
CSD 200/300/400/500 DYNAMOMETER
NK GRASP SENSOR, MODEL GA002
NK GRASP SENSOR, MODEL GA001
NK DIGI-GRIP SENSOR, MODEL DGR001
DMG100 AND 500 ISOMETRIC STRENGTH DYNAMOMETER
REMUSK MP
CLINCAL HAND MASTER SYSTEM MODEL # EXH9000-002
NK DYNA-GRIP SENSOR, MODEL DG001
TECH DYNE - HP-2000, SKREEN TEST, RMS-200
CLINICAL HANDMASTER SYSTEM OR CHMS
NK PINCH SENSOR, MODEL PA001
PINCH SENSOR, MODEL PF001
NK PINCH SENSOR, MODEL PF002
NK DEVIATION SENSOR, MODEL DV001
NK GRASP SENSOR, MODEL GR001
NK PINCH SENSOR, MODEL PA002
GS-220 HAND IMPAIRMENT EVALUATION SYSTEM
ELECTRO-GONIOMETER DIAGNOSTIC DEVICE
GREENLEAF HAND IMPAIRMENT EVALUATION SYSTEM
MUSCLE EXAMINATION & EXERCISE DOSIMETER (MEED) SYS
KIN-COM JR
DYNATRON II
FORCE EVALUATION AND TESTING SYSTEM (FETS)
DIGITAL GRIP/PINCH STRENGTH METOR
MED-EX
MYO-METRIC II

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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