Global partners
Distribution, built on the paperwork nobody wants to do.
We design powered mobility devices in Perth and work with distributors, rehabilitation suppliers and OEM partners in other markets. Every market has its own regulator, and that is usually the part that stalls a partnership. We do that work with you rather than handing it over.
What we offer
Four things we bring to the table.
Regulatory work we do with you
CE, TGA and FDA pathways are part of our engineering process, not an afterthought. We hold the technical files and conformity documentation, and prepare submissions alongside your local regulatory consultant rather than leaving you to reverse-engineer them.
Products engineered for real footpaths
Kerb climb, cross-camber stability, sealed drivetrains for coastal and humid climates. Specifications are published and tested to the ISO 7176 series, so your clinical assessors can cite real figures.
Parts and service you can actually promise
Common components across platforms, published spare part lists, and controllers that can be re-parameterised in the field. A distributor cannot sell a chair it cannot repair.
OEM and ODM programmes
Where the fit is right, we develop under a partner's own brand: seating, colourways, control configurations and documentation in your market's language and format.
Market access
Regulatory frameworks we work within.
- Australia
- TGA — ARTG inclusion
- Supplying
- European Union
- EU MDR — CE marking
- United States
- FDA — 510(k) / listing
- United Kingdom
- MHRA — UKCA
- Other markets
- Assessed case by case
- On request
Status is stated per market and per device. Ask us for the current position on a specific model before you plan a launch, and we will send the conformity documentation we hold.
Who we work with
What makes a partnership work.
Clinical capability, not just logistics
Powered mobility is prescribed, not merely sold. Partners who employ or work closely with occupational therapists get better outcomes and far fewer returns.
A service capability on the ground
Stock holding for consumables and batteries, a technician who can attend, and a response time you are willing to publish.
Regulatory literacy in your market
You do not need an in-house regulatory team, but you do need to know which pathway applies and who signs off on it locally.
Willingness to feed information back
Field failures, footpath conditions, seating problems. Most of our engineering improvements started as a distributor's complaint.
How it starts
From first email to first order.
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Tell us your market
Territory, segments you sell into, and the regulatory pathway that applies where you are. We reply with what we can and cannot supply into that market today.
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Technical and regulatory review
We share specifications, test reports and the conformity documentation we hold, so you can assess the gap to local approval before either side commits.
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Samples and clinical trial
Evaluation units for assessment by your clinical team, in the environments your customers actually use.
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Commercial terms
Territory, volumes, pricing, warranty handling and service obligations, in writing.
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Launch support
Product training for your clinical and service staff, documentation in your format, and a named contact here.
Tell us your market.
Send the territory you cover, the segments you sell into, and the regulatory pathway that applies where you are. We will reply with what we can and cannot supply into that market today.
Regulatory status, product availability and specifications differ by market and are subject to change. Nothing on this page is an offer to supply or a representation that a given device is approved for sale in a particular jurisdiction. Distribution is subject to a written agreement.