|Exposing the LASIK Scam
|FDA MDR against NIDEK
|Page 1 of 1|
|Author:||Broken Eyes [ Wed Dec 14, 2005 1:48 am ]|
|Post subject:||FDA MDR against NIDEK|
http://www.accessdata.fda.gov/scripts/c ... _ID=558775
"Had bilateral lasik. Vision has been impaired, severe dry eyes, severe night vision problems. Induced irregular astigmatism in patient's corneas."
For more medical device reports filed against NIDEK, go to the following link and type in NIDEK for the manufacturer and LZS for the product code:
http://www.accessdata.fda.gov/scripts/c ... hoptions=1
|Author:||Broken Eyes [ Sun Oct 21, 2007 9:20 pm ]|
http://www.accessdata.fda.gov/scripts/c ... _ID=902835
While using the nidex diode laser, the pts are experiencing pain, when there should be none. The power output has been checked by in-house bmet and by nidex and are within specifications. The laser has been changed, and the dual delivery slit lamp/ indirect switch box has been changed. The pattern of the laser beam appears to concentrate the laser power towards the center of the beam, rather than be evenly distributed.
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