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

Back to MHRA

Manufacturer's Devices - Tekia Inc

Address:

17 Hammond Street Suite 414

Irvine

California 92618

United States

Authorised Representative/ UK Responsible Person
Name: International Associates Limited
Address:

38 Queen Street

Glasgow

G1 3DX

Scotland United Kingdom

Code/Term Type

Posterior-chamber intraocular lens pseudophakic Posterior-chamber intraocular lens pseudophakic Class IIb

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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