Your FDA laser light show annual report

This free tool prepares and submits your FDA annual report, the filing that keeps your laser light show variance active. It's due September 1 each year and takes about 10 minutes. When you're done, X-Laser reviews your answers and submits the report to the FDA on your behalf, and you'll be CC'd on the email to the FDA.

Question 1 of 3

Have you received a complaint or warning letter from the FDA about laser safety procedures in the past year?

Question 2 of 3

Do you use any high-powered lasers other than X-Laser or LaserCube models or do you use any Laser Illuminated Lighting Instruments (LILI) systems other than the Elation Proteus Radius and Atlas?

Question 3 of 3

Are you still in business and using your X-Laser system(s) under your variance?