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 - L'Amy America

Address:

40 Richards Avenue Norwalk

Norwalk

Connecticut 06854 USA

United States

Authorised Representative/ UK Responsible Person
Name: Suzanne Taylor-Turnbull
Address:

Herford Cottage Bull in the Oak

Market Bosworth Cadeby

Nuneaton

warwickshire CV13 0DW

England United Kingdom

Code/Term Type

Prescription spectacles Prescription spectacles Class I

Tinted non-prescription spectacles Tinted non-prescription spectacles 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
Prescription spectacles	Prescription spectacles	Class I
Tinted non-prescription spectacles	Tinted non-prescription spectacles	Class I