Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - SPIO Inc.

Address:

127 SW 156th St.

Burien

Washington 98166

United States

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Wrist/hand orthosis Wrist/hand orthosis Class I

Multiple-joint arm orthosis Multiple-joint arm orthosis Class I

Multiple spinal region orthosis Multiple spinal region orthosis Class I

Multiple-joint lower limb orthosis Multiple-joint lower limb orthosis Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Wrist/hand orthosis	Wrist/hand orthosis	Class I
Multiple-joint arm orthosis	Multiple-joint arm orthosis	Class I
Multiple spinal region orthosis	Multiple spinal region orthosis	Class I
Multiple-joint lower limb orthosis	Multiple-joint lower limb orthosis	Class I