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Regulatory Requirements

DB Orthodontics ensures that its orthodontic and dental products meet the European Regulatory requirements detailed in MDD 93/42/EEC, as amended by Directive 2007/47/EC, the United States Medical Device Regulations (21 CFR Part 820) and the Canadian MDR (SOR/98-282) as applicable.

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Stop The Snoring: Help Your Patients Get a Good Nights Sleep

In this blog, we explain how Leone’s Mandibular Advancement Device offers a higher level of comfort for the patient than many models on the market,... Read more

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As a member of the British Dental Industry Association, DB Orthodontics supports the industry’s Counterfeit and Substandard Instruments and Device Initiative (CSIDI). For more information and useful tips on spotting counterfeit dental devices visit the BDIA website.