Dualer IQ Pro Primary Inclinometer

FDA UDI

Class I (US FDA UDI)

by J-Tech Medical, Inc.

Identity

Trade Name: Dualer IQ Pro Primary Inclinometer FDA UDI
Generic Name: Electronic goniometer/kinesiology sensor FDA UDI
Device Name: A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient. FDA UDI
Model / Reference: 9CM113 FDA UDI
Description: A device to assist the clinician with establishing an objective assessment of a person’s range of movement. The device is intended to be non-invasive, non-surgical and transient. FDA UDI

Identifiers

Primary DI / UDI-DI: G0419CM1130 FDA UDI
FDA Product Code: KQX FDA UDI
GMDN Term: Electronic goniometer/kinesiology sensor FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.1500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Electronic goniometer/kinesiology sensor

Dualer IQ Pro Primary Inclinometer by J-Tech Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electronic goniometer/kinesiology sensor.

myrecovery, myrecovery App & Dashboard, myrecovery Patient Engagement & Outcomes — FUTURE HEALTH WORKS LTD · Class I
ROMI Dual Inclinometer System — Lafayette Instrument Company · Class I
E-LINK N100 Small Goniometer — BIOMETRICS LIMITED · Class II
XACT Robotics: Respiration Sensor All Around Strap — XACT ROBOTICS LTD · Class II
MotionSense Knee Alignment Block — ENMOVI LTD · Class I
MotionSense Knee Alignment Block — ENMOVI LTD · Class I
Titronics — Titronics Research & Development Co. · Class I
Digital Knee® — OPUM TECHNOLOGIES SERVICES LIMITED · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: J-Tech Medical, Inc.

Sources (1)

FDA UDI 108c16ff-2622-4206-844f-a439adcd9c6a 34 fields · synced Jun 6, 2026