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Adverse-event reports (MAUDE)

Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.

No adverse-event reports are linked to this device.

Recall history

No recalls linked.

Regulatory clearances

None linked.

Manufacturer compliance record
DateTypeOutcomeFacilityCitations
2025-05-01NAINo action indicatedAlcon Research, LLC0
2024-06-12VAIVoluntary action indicatedAlcon Research, LTD.0
2023-02-03NAINo action indicatedCiba Vision GmbH0
2022-09-15NAINo action indicatedAlcon Research, LLC0
2022-09-15NAINo action indicatedAlcon Research, LLC0
2022-08-26VAIVoluntary action indicatedPt Ciba Vision Batam0
2021-08-24NAINo action indicatedAlcon Research LLC0
2019-12-05NAINo action indicatedAlcon Research, LLC1
2019-11-21NAINo action indicatedAlcon Laboratories Ireland, Ltd0
2019-10-24NAINo action indicatedAlcon Research LLC0
2018-03-19NAINo action indicatedAlcon Research Ltd0
2017-01-17NAINo action indicatedAlcon Research LLC0
2017-01-17NAINo action indicatedAlcon Research LLC0
2016-11-17VAIVoluntary action indicatedCIBA VISION Johor Sdn. Bhd.2
2016-07-07VAIVoluntary action indicatedAlcon Laboratories Ireland, Ltd2
2016-05-04VAIVoluntary action indicatedAlcon Research, LLC0
2016-01-28NAINo action indicatedAlcon Research LLC0
2016-01-21NAINo action indicatedAlcon Research, LLC0
2015-09-11VAIVoluntary action indicatedWavelight GmbH1
2015-09-02NAINo action indicatedAlcon Research, LLC0
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