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 - NovaBone Products LLC

Address:

13510 NW US Highway 441

Alachua

32615

United States

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

General oral wound dressing animal-derived General oral wound dressing animal-derived Class III

Dental material injection cannula reusable Dental material injection cannula reusable Class I

Dental bone matrix implant synthetic Dental bone matrix implant synthetic Class III

Bone matrix implant synthetic non-antimicrobial Bone matrix implant synthetic non-antimicrobial Class III

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
General oral wound dressing animal-derived	General oral wound dressing animal-derived	Class III
Dental material injection cannula reusable	Dental material injection cannula reusable	Class I
Dental bone matrix implant synthetic	Dental bone matrix implant synthetic	Class III
Bone matrix implant synthetic non-antimicrobial	Bone matrix implant synthetic non-antimicrobial	Class III