Glaukos Corporation
FDA adverse event reports naming Glaukos Corporation as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: GLAUKOS CORPORATION.
- Total reports
- 1,404
- Deaths
- 0
- Injuries
- 926
- Malfunctions
- 478
Reports per year
213
714
2215
8316
9917
14918
16019
12020
14321
13822
14623
14824
12525
6226
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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