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2022 Conference Committee

ALD Organization Disclosure - Disclaimer on Protocols and Opinions

The views expressed and opinions and materials presented during a presentation represent the personal views and opinions of the individual speakers and do not necessarily represent the views and opinions of the Academy of Laser Dentistry. The Academy of Laser Dentistry assumes no responsibility for the content of the presentations made by individual speakers pertaining to protocols for laser treatment. Any suggested protocols for treatment may be based upon the speakers' own clinical experience and should not be construed as Academy of Laser Dentistry recommended protocols.

Note: These presentations discuss investigational devices that may not yet have received U.S. FDA approval or clearance for the specified clinical indications, or describes off-label uses.

The Academy of Laser Dentistry (ALD) is a not-for-profit organization qualifying under Section 501c(3) of the U.S. Internal Revenue Code.The Academy of Laser Dentistry is an international professional membership association of dental practitioners and supporting organizations dedicated to improving the health and well-being of patients through the proper use of laser technology. The Academy is dedicated to the advancement of knowledge, research, and education and to the exchange of information relative to the art and science of the use of lasers in dentistry.  Abstracts, presenter biographies, disclosure information, and product descriptions are published for educational purposes as submitted by the respective presenters and exhibitors. They do not necessarily represent the views of the Academy of Laser Dentistry. ALD is not responsible for the opinions expressed by the presenters, exhibitors, and advertisers.  Written permission must be obtained by the Academy to audiotape, videotape, duplicate, and/or distribute any portion of the conference program or proceedings.  The ALD Conference presents opportunities that may discuss investigational devices that have not yet received U.S. FDA approval or clearance for the specified clinical indications or describes off-label uses. Practitioners are advised to investigate and consider which medical devices and materials are cleared by the U.S. Food and Drug Administration for safety and efficacy and which are considered experimental, and which procedures are within the applicable scope of their license, competence, skills, and abilities, as established by their education, training, and experience. Clinicians are advised to review the specific indications for use of their devices and to review their operator manuals for guidance on operating parameters before attempting similar techniques on their patients.

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