FDA
The FDA has advisories and info about Lasik. Any ideas how we can send them info about ENS?

I am confused about FDA regulation, since below it says it does not cover Medical Practice, which is under State Board Certification. That is weird, since Lasik is done by certified doctors... It is unfair to have to report to the medical board, who are probably all doctors themselves. I need to ask someone about this. What products does FDA regulate? Consumers can play an important public health role by reporting to FDA any adverse reactions or other problems with products the agency regulates. FDA is responsible for ensuring that foods are safe, wholesome, and correctly labeled. It also oversees medicines, medical devices (from bandages to artificial hearts), blood products, vaccines, cosmetics, veterinary drugs, animal feed, and electronic products that emit radiation (such as microwave ovens and video monitors), ensuring that these products are safe and effective. Why should I report? The testing that helps to establish the safety of products, such as drugs and medical devices, is typically conducted on small groups before FDA approves the products for sale. Some problems can remain unknown, only to be discovered when a product is used by a large number of people. When problems with FDA-regulated products occur, the agency wants to know about them and has several ways for the public to make reports. Timely reporting by consumers, health professionals, and FDA-regulated companies allows the agency to take prompt action. The agency evaluates each report to determine how serious the problem is, and, if necessary, may request additional information from the person who filed the report before taking action. How do I report an emergency? If the situation is an emergency that requires immediate action, such as a case of food-borne illness or a drug product that has been tampered with, call the agency's main emergency number, staffed 24 hours a day, 301-443-1240. You also can report emergencies, as well as non-emergencies, to the FDA consumer complaint coordinator in your geographic area. Situations that do not require immediate action--such as a non-emergency adverse reaction to a food product or an over-the-counter medical device that doesn't work as advertised--can be reported either to the appropriate consumer complaint coordinator or to the FDA office that handles the product. How do I report non-emergencies about medical products: medicines, medical devices, blood products, biologics, special nutritionals? MedWatch -- The FDA Safety Information and Adverse Event Reporting Program allows healthcare professionals and consumers to voluntarily report serious problems that they suspect are associated with the drugs and medical devices they prescribe, dispense, or use. These problems include serious adverse reactions and events, product quality problems, and product use errors. Reporting can be done online, by phone, or by submitting the MedWatch 3500 form by mail or fax. Visit the MedWatch How To Report page for more details. What should I include in my report? Report what happened as soon as possible. Give names, addresses and phone numbers of persons affected. Include your name, address and phone number, as well as that of the doctor or hospital if emergency treatment was provided. State the problem clearly. Describe the product as completely as possible, including any codes or identifying marks on the label or container. Give the name and address of the store where the product was purchased and the date of purchase. You also should report the problem to the manufacturer or distributor shown on the label and to the store where you purchased the product. Top What kinds of problems doesn’t FDA handle and where can I report them? Reports and complaints about the following should be made to the agencies listed. Phone numbers can be found in your local phone directory: Restaurant food and sanitation--Local or state health departments Unsolicited products in the mail--U.S. Postal Service Accidental poisonings--Poison control centers or hospitals Pesticides or air and water pollution--U.S. Environmental Protection Agency Hazardous household products (including toys, appliances, and chemicals)--Consumer Product Safety Commission, 1-800-638-2772 Alcoholic beverages--Department of Treasury's Bureau of Alcohol, Tobacco and Firearms Drug abuse and controlled substances--Department of Justice's Drug Enforcement Administration Hazardous chemicals in the workplace--Department of Labor's Occupational Safety and Health Administration Warranties--Federal Trade Commission Dispensing and sales practices of pharmacies--State board of pharmacy Medical practice--State certification board

It looks like Lasik falls under the FDA for being a cosmetic or medical device, not something regulated by the state medical certification boards. So that is why they have had more luck in complaining and getting publicity. We all have to complain to our separate state medical boards, who are probably doctors themselves. I wish there were more of a unified federal government check on medical practices - maybe Dept. of Health?