ALCON CILCO POSTERIOR CHAMBER LENS
by Unknown
The ALCON CILCO POSTERIOR CHAMBER LENS by Unknown has a safety score of 83 out of 100, placing it in the low-risk category. Based on FDA MAUDE data, there have been 28 adverse event reports since its introduction in 2015. With an estimated 0 units in use, the incident rate is 0 per 10,000 units. It ranks #3 out of 54 devices in the Ophthalmic category.
Adverse Events
Total reports filed with FDA MAUDE
Death Reports
Death reports associated with device
Incident Rate
Per 10,000 units in use
Recalls
No recalls on record
Estimated Units in Use
Based on market data estimates
Category Ranking
In Ophthalmic by safety score
How This Compares
Other Ophthalmic Devices
HEYER-SCHULTE
Unknown
AMO ARRAY MULTIFOCAL LENS
Unknown
HYDROVIEW INTRAOCCULAR LENS
Unknown
INTRAOCULAR LENS
Unknown
Important Context
Adverse event reports reflect reported incidents, not confirmed device failures. Higher numbers may indicate greater device usage, better reporting systems, or increased awareness. This data should be one factor in your research — always consult your physician.