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 - KometaBio Inc.

Address:

One Bridge Plaza North Suite 275

Fort Lee

New Jersey 07024

United States

Authorised Representative/ UK Responsible Person
Name: Regen Marketing Limited
Address:

Ivy Cottage Bridgnorth Road

Stourton

Stourbridge

DY75BH

England United Kingdom

Code/Term Type

Manual bone mill Manual bone mill 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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