Cadense

FDA UDI

Class I (US FDA UDI)

by Cadense Inc

Identity

Trade Name: Cadense FDA UDI
Generic Name: Orthotic shoe, non-customized FDA UDI
Device Name: Cadense AERIOs are adaptive sandal-slide hybrids designed to help with walking difficulties in a warm-weather format. Built with the same Variable Friction Technology as the Cadense Originals, they support smoother movement and greater ease on multiple surfaces. AERIOs feature a removable backstrap, adjustable front closure, and a supportive sole engineered for daily comfort. This versatile style offers an accessible option for those seeking adaptable footwear without compromising on functionality or design. FDA UDI
Model / Reference: AERIO Men's R1 FDA UDI
Description: Cadense AERIOs are adaptive sandal-slide hybrids designed to help with walking difficulties in a warm-weather format. Built with the same Variable Friction Technology as the Cadense Originals, they support smoother movement and greater ease on multiple surfaces. AERIOs feature a removable backstrap, adjustable front closure, and a supportive sole engineered for daily comfort. This versatile style offers an accessible option for those seeking adaptable footwear without compromising on functionality or design. FDA UDI

Identifiers

Primary DI / UDI-DI: 00810195430588 FDA UDI
FDA Product Code: KNP FDA UDI
GMDN Term: Orthotic shoe, non-customized FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.3475 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

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

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Expiration Date

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Manufacturing Date

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Category: Orthotic shoe, non-customized

Cadense by Cadense Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Cadense Inc

Sources (1)

FDA UDI 0710c19a-2289-4487-8d7e-918a9d9dde36 34 fields · synced May 30, 2026