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Kaydiar Medical

United Kingdom (ex Northern Ireland)·UK-MF-000043517

Last updated September 18, 2026

About

Explore Kaydiar’s innovative offloading solutions for wound and foot pressure relief, including customizable insoles and advanced orthotic technology for clinical and personal care.

From the manufacturer's own website. Source

What Kaydiar Medical makes

Kaydiar Medical produces offloading solutions designed for wound and foot pressure relief, including customizable insoles and orthotic devices. These products are intended for clinical and personal use to reduce pressure on vulnerable areas, particularly for patients with wounds or foot-related conditions.

The company’s devices fall under EU Class I medical device regulations and are registered in the EU’s eudamed database. Kaydiar Medical is based in the United Kingdom.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Kaydiar Medical manufacture?

Kaydiar Medical specialises in offloading solutions for wound and foot pressure relief. Their portfolio includes customisable insoles and advanced orthotic devices, designed to reduce pressure on vulnerable areas—particularly for patients with wounds or foot-related conditions. These products are intended for both clinical and personal use.

Where is Kaydiar Medical based?

Kaydiar Medical is based in the United Kingdom. The company’s headquarters and operations are located there, though specific regional offices or manufacturing sites are not detailed in the available information.

Which regulatory registries list Kaydiar Medical’s devices?

Kaydiar Medical’s devices are listed in the eudamed database, which is the official EU registry for medical devices. This registration is required for devices marketed within the European Economic Area under EU medical device regulations.

How are Kaydiar Medical’s devices classified under EU regulations?

Kaydiar Medical’s devices fall under EU Class I classification. This classification is typically assigned to low-risk medical devices, such as certain orthotic insoles and offloading solutions, which pose minimal risk to patients when used as intended.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United Kingdom (ex Northern Ireland)
Address
Gwynnant, Coedffaldau Road, , Swansea, United Kingdom (ex Northern Ireland)
Facebook
—
Phone
+44 (0) 7552 140 218
PRRC Contact
David Barton
EUDAMED SRN
UK-MF-000043517
FDA FEI Number
—
DUNS Number
—

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Kaydiar Ltd DS002
EUDAMED
Class IActive
Kaydiar Ltd DS001
EUDAMED
Class IActive
Zerosole ZS001
EUDAMED
Class IActive

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