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 - Implanet

Address:

Technopole Montesquieu Allée François Magendie

Martillac

33650

France

Authorised Representative/ UK Responsible Person
Name: Osteon Medical Ltd
Address:

133 Tame Road Birmingham

Birmingham

B67DG

England United Kingdom

Code/Term Type

Bone-screw internal spinal fixation system sterile Bone-screw internal spinal fixation system sterile Class IIb

Hard-tissue ultrasonic surgical system Hard-tissue ultrasonic surgical system 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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Code/Term		Type
Bone-screw internal spinal fixation system sterile	Bone-screw internal spinal fixation system sterile	Class IIb
Hard-tissue ultrasonic surgical system	Hard-tissue ultrasonic surgical system	Class IIb