WAVELIGHT FS200 FEMTOSECOND LASER
Received Jun 17, 2026
Report 3003288808-2026-00279 · MDR key 25529867
Device
Generic name
Ophthalmic Laser
Manufacturer
Wavelight GmbhModel number
NACatalog number
8065000123
Lot number
14UPFA
Product problems
- Unexpected Therapeutic Results
Patient
38 YR · Female
- Insufficient Information
Narrative
Description of Event or Problem
A PHYSICIAN REPORTED THAT DOCTOR NOTICED NO SIDE CUT IN THE RIGHT EYE OF THE PATIENT DURING REFRACTIVE SURGERY AND DECIDED TO ALLOW THE EYE TO HEAL FOR RETREATMENT AGAIN IN FEW WEEKS. THE PROCEDURE WAS NOT COMPLETED. THERE ARE TWO RELATED REPORTS FOR THIS PATIENT. THIS REPORT ADDRESSES THE PATIENT'S RIGHT EYE AND ANOTHER MANUFACTURER REPORT WILL BE FILED FOR THE FELLOW EYE.
Additional Manufacturer Narrative
H.3., H.6.: INVESTIGATION, INCLUDING ROOT CAUSE ANALYSIS, IS IN PROGRESS. A SUPPLEMENTAL MDR WILL BE FILED AS NECESSARY IN ACCORDANCE WITH 21 CFR 803.56 WHEN ADDITIONAL REPORTABLE INFORMATION BECOMES AVAILABLE. THE MANUFACTURER INTERNAL REFERENCE NUMBER IS: (B)(4).