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 - Tenex Health Inc

Address:

26902 Vista Terrace

Lake Forest

CA 92630

United States

Authorised Representative/ UK Responsible Person
Name: Donawa Lifescience Ltd
Address:

Aviation Business Park Enterprise Close

Christchurch

BH23 6NX

England United Kingdom

Code/Term Type

Hard-tissue ultrasonic surgical system Hard-tissue ultrasonic surgical system Class IIa

Hard-tissue ultrasonic surgical system Hard-tissue ultrasonic surgical system Class IIa

Contact details

Freedom of information

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

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Hard-tissue ultrasonic surgical system	Hard-tissue ultrasonic surgical system	Class IIa
Hard-tissue ultrasonic surgical system	Hard-tissue ultrasonic surgical system	Class IIa