The people of Spex are what sets us apart!
Our team is a creative bunch of solution finders, passionate about helping others, and being a happy and positive light in the world of those we are privileged to work with.
Spex accomplishes what the seating clinician desires, and what the user needs. Distinguished by high standards of design and clinical evaluation, Spex delivers an uncompromising seating choice packed with clever advantages. The experience of working with Spex Seating provides a blend of form and function.
Spex is dedicated to protecting our environment and ensuring a clean future for our descendants.
You can have confidence in Spex Seating’s management of environmental aspects and impacts associated with the manufacture and supply of equipment for people with postural and physical challenges.
As a caring, corporate citizen, Spex supports the responsible stewardship of the earth, its inhabitants and resources.
Our products are designed to last, and their manufacture, use and disposal embody the environmental principles of Reduce, Reuse and Recycle.

Spex Limited operates a Quality Management System certified to ISO 13485:2016 — Medical Devices — Quality Management Systems — Requirements for Regulatory Purposes. Download our ISO 13485 Certificate. Our Quality Policy is available on request.
Spex Seating has been assessed by iPRO for modern slavery risks, including Forced Labour, Child Labour, Human Trafficking and Policies & Procedures.
European Union (EU)
Our products comply with Regulation (EU) 2017/745 on Medical Devices (MDR). Where applicable, products are CE marked to demonstrate conformity with relevant requirements. Declaration of Conformity is available on request.
United States of America (US)
Spex Limited products sold in the United States are Class I medical devices listed with the United States Food and Drug Administration (FDA) as exempt from premarket notification [510(k)], unless otherwise stated.
Australia
Our products are included in the Australian Register of Therapeutic Goods (ARTG) where applicable and comply with the Therapeutic Goods Act 1989 and associated regulations.
New Zealand
Spex Limited complies with applicable requirements under the Medicines Act 1981 and Medical Devices Regulations in New Zealand.
Taiwan
Our products are distributed in Taiwan in compliance with local regulatory requirements through our authorised local distributor.
Product Claims and Intended Use
All product information provided by Spex Limited, including on this website, is consistent with the Intended Use as specified in the product’s Technical Documentation and regulatory submissions. Spex Limited does not make claims beyond those supported by product documentation and regulatory approvals.

We pride ourselves in uncompromised quality.
Spex Seating’s operations centre has achieved ISO 13485:2016 certification. You can have confidence that Spex Seating’s Quality Management System ensures we will supply wheelchair seating and support products that will consistently meet your requirements.
To maintain customer confidence in Spex Seating’s effectiveness, Telarc regularly reviews our management system for compliance with standards.
At Spex Seating, we’re committed to delivering products that meet the highest standards for safety, performance, and clinical quality. Our seating systems are tested to international regulations, giving you total confidence in every product we make. Below is a summary of the key standards that specific products in the Spex range comply with.
Crash-Tested for Transport Safety
Tested to:
- RESNA WC-4, Section 20
- ISO 16840-4
Ensuring our seating systems are safe for use in motor vehicles during transportation.
Designed for Real-World Use
Tested to:
- ISO 21856 – Assistive Products General Requirements
- ISO 16840-3 – Structural Strength Testing for Postural Support Devices
Focused on ease of use, user safety, and durability.
Tested for Ignition and Flame Resistance
Tested to:
- ISO 16840-10
- California Technical Bulletin 117
- EN1024 Part 1 and 2
Testing for ignitability and burning behaviour in materials used across our seating range.
Eligible for Medicare Reimbursement (USA)
Some cushion models are reviewed by PDAC contractors, enabling Medicare/Medicaid reimbursement.
Conformity with Global Medical Standards
CE marked products are in conformity with the requirements of the EU Medical Devices Regulation (EU) 2017/745