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 - Ortholese Limited

Address:

Basepoint Business & Innovation Centre 110 Butterfield

Great Marlings

Luton

Bedfordshire LU2 8DL

United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Cervicothoracolumbosacral spine orthosis rigid Cervicothoracolumbosacral spine orthosis rigid Class I

Ankle/foot orthosis Ankle/foot orthosis Class I

Knee/ankle/foot orthosis Knee/ankle/foot orthosis Class I

Foot orthosis Foot orthosis Class I

Elbow orthosis Elbow orthosis Class I

Elbow/wrist/hand orthosis Elbow/wrist/hand orthosis Class I

Hip/knee/ankle/foot orthosis Hip/knee/ankle/foot orthosis Class I

Ankle joint orthosis Ankle joint 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
Cervicothoracolumbosacral spine orthosis rigid	Cervicothoracolumbosacral spine orthosis rigid	Class I
Ankle/foot orthosis	Ankle/foot orthosis	Class I
Knee/ankle/foot orthosis	Knee/ankle/foot orthosis	Class I
Foot orthosis	Foot orthosis	Class I
Elbow orthosis	Elbow orthosis	Class I
Elbow/wrist/hand orthosis	Elbow/wrist/hand orthosis	Class I
Hip/knee/ankle/foot orthosis	Hip/knee/ankle/foot orthosis	Class I
Ankle joint orthosis	Ankle joint orthosis	Class I