Wavelight Gmbh
FDA adverse event reports naming Wavelight Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: WAVELIGHT GMBH.
- Total reports
- 13,877
- Deaths
- 0
- Injuries
- 9,853
- Malfunctions
- 4,009
Reports per year
50412
82413
1,66714
1,24315
1,08716
1,74317
1,89818
1,26819
81820
46721
31022
31323
35424
61025
31126
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Excimer Laser SystemLZS8,913
- Powered Laser Surgical InstrumentGEX4,218
- Ophthalmic Femtosecond LaserOOE712
- Intraocular LensHQL12
- Device, Analysis, Anterior SegmentMXK9
- Topographer, Corneal, Ac-PoweredMMQ7
- Biomicroscope, Slit-Lamp, Ac-PoweredHJO2
- Pump, Infusion, InsulinLZG2
- Product code 2992991
- Aberrometer, OphthalmicNCF1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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