myrecovery, myrecovery App & Dashboard, myrecovery Patient Engagement & Outcomes

FDA UDI

Class I (US FDA UDI)

by Future Health Works Ltd

Identity

Trade Name: myrecovery, myrecovery App & Dashboard, myrecovery Patient Engagement & Outcomes FDA UDI
Generic Name: Electronic goniometer/kinesiology sensor FDA UDI
Device Name: A clinical information system with a digital goniometer. The system can be configured to have diagnostic functionality but does not allow or enable direct diagnosis. No decisive information for making a diagnosis can be provided by the system on its own and it cannot provide diagnosis by itself, nor does it perform as a clinician or provide an indicative diagnosis to the lay user. FDA UDI
Model / Reference: MD FDA UDI
Description: A clinical information system with a digital goniometer. The system can be configured to have diagnostic functionality but does not allow or enable direct diagnosis. No decisive information for making a diagnosis can be provided by the system on its own and it cannot provide diagnosis by itself, nor does it perform as a clinician or provide an indicative diagnosis to the lay user. FDA UDI

Identifiers

Primary DI / UDI-DI: G333KQX001 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Electronic goniometer/kinesiology sensor

myrecovery, myrecovery App & Dashboard, myrecovery Patient Engagement & Outcomes by Future Health Works Ltd — Class I — FDA UDI — listed in FDA GUDID

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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

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Manufacturer

Manufacturer: Future Health Works Ltd

Sources (1)

FDA UDI 8e6750bc-adec-4497-969d-e87a49bdcb85 33 fields · synced May 30, 2026