The FDA has authority over use of devices used to perform laser eye surgery. They are aware that prospective LASIK patients are not being adequately warned of the risks. In July 2022, the FDA actually proposed guidance to potential Lasik patients. See the Press Release Here.
On July 28, 2022, the FDA announced:
FDA Seeks to Improve Patient Communication on LASIK Benefits and Risks Through Issuance of Draft Guidance
https://www.regulations.gov/comment/FDA-2022-D-1253-0343
https://www.regulations.gov/comment/FDA-2022-D-1253-0361
https://www.regulations.gov/comment/FDA-2022-D-1253-0391
https://www.regulations.gov/comment/FDA-2022-D-1253-0396
https://www.regulations.gov/comment/FDA-2022-D-1253-0401
https://www.regulations.gov/comment/FDA-2022-D-1253-0408
https://www.regulations.gov/comment/FDA-2022-D-1253-0410
https://www.regulations.gov/comment/FDA-2022-D-1253-0456
https://www.regulations.gov/comment/FDA-2022-D-1253-0452
https://www.regulations.gov/comment/FDA-2022-D-1253-0465
https://www.regulations.gov/comment/FDA-2022-D-1253-0582