Originally Posted by
X-Laser
A fair point Frank but I would make two counters:
1) While the FDA does not "approve" lasers as they do drugs, they do approve of their entry into US commerce via approval of the manufacturer's product report.While of course I agree that they do not typically test models before sale as would normally be done in again say a drug approval process, they do careful review detailed product reports to ensure that manufacturers are doing things safety and approve the filing... when then approves the laser for introduction into commerce. That level of granularity more than most people care about but since the letter that comes from FDA both means and literally says "approved," I think that calling something FDA approved is a fair if not perfectly accurate shorthand.
Secondly, a number of the shows in Europe carefully control their irradiance levels to avoid practically unsafe exposures... I say practically rather than academically because I am not going to sit here and say that everyone follows MPE. That said, a large and growing number of people do try to stick to MPE rules and in any case, without someone having the experience to quantify and mitigate the hazard how would an end user ever know what is safe and what is not?.
A a followup to that, a number of people are somewhat quietly but realistically concerned that many of these shows are actually causing subtle injuries which will show up later in life or may later be exacerbated by other factors. Occult injuries I believe they are called which are not immediately obvious and are corrected for by the brain or not severe enough yet to cause trouble. The FDA's perspective is that an occult injury is still an injury and that seems reasonable to me. However, as you say, there are reasonably few "bodies" so who am I to say for sure?