Medifirst Solutions Inc. updated the progress of its 510(k) submission to the Food and Drug Administration (FDA). Working with Medifirst's FDA consulting firm, the company is progressing to gather the information and reports necessary to respond to the request for additional information regarding the hand-held laser system received from the FDA. The deadline for the company to respond is June 2016, but Medifirst anticipates it will have the response completed within the next eight weeks.

Upon the completion of the review process to the satisfaction of the FDA, and being awarded 510(k) clearance, Medifirst will begin to sell its laser units across the United States. The company believes that the approval will also jump-start international sales for several distributors in South America and Europe.