Intraocular Pressure Lowering Implant
Adverse-event figures are drawn from the U.S. Food & Drug Administration (FDA) MAUDE database, refreshed March 2026, see our methodology.
OpenFDA device adverse-event casebook.
FDA MAUDE casebook
openFDA event book Intraocular Pressure Lowering Implant LIGHT-BOOK · MAUDE
#436 of 1000 · 2,671 reports · 2007–2026
- BOOK 2,671 reports
- RANK #436 of 1000
- DEATH 0 death-typed
- INJ 2,014 injury-typed
- MALF 657 malfunction
- SPAN 2007–2026
- PEAK 2018: 511
- PHOTO Prosthesis
Nearest event-volume peer: Prosthesis, Hip, Hemi-, Femoral, Metal (12 report gap)
Intraocular Pressure Lowering Implant sits #436 of 1000 among tracked device types with 2,671 MAUDE reports spanning 2007–2026. Rank counts report volume, not confirmed device fault. Event_type Death / Injury / Malfunction are one code per report — not the same population as patient-outcome rows ( methodology). Read with this device → · Lead manufacturer → · Similar-volume device →
Injury-coded reports run above the device-type norm
Intraocular Pressure Lowering Implant carries 75.4% INJURY-coded reports, 45.1pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 0.0% corpus 1.5% · below corpus mean (-1.5 pp)
- INJ 75.4% corpus 30.3% · above corpus mean (+45.1 pp)
- MALF 24.6% corpus 64.8% · below corpus mean (-40.2 pp)
Lead product-problem code Adverse Event Without Identified Device or Use Problem is 44% of coded problems · Lead manufacturer ALCON RESEARCH, LLC - ALCON PRECISION DEVICE accounts for 100% of manufacturer-tagged reports · Top event location I is 60% of location-tagged rows .
Intraocular Pressure Lowering Implant in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Forceps
Forceps, Biopsy, Non-Electric
2,705 reports
- Prosthesis
Prosthesis, Hip, Hemi-, Femoral, Metal
2,683 reports
- Intraocular P… (this)
Intraocular Pressure Lowering Implant
2,671 reports
- System
System, Imaging, Pulsed Doppler, Ultrasonic
2,659 reports
- Staple
Staple, Fixation, Bone
2,647 reports
- Handpiece
Handpiece, Contra- And Right-Angle Attachment, Dental
2,629 reports
What this shows Intraocular Pressure Lowering Implant carries 2,671 MAUDE reports, ranked #436 of 1000.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Top Product Problems
Yearly Trend
Reports in 2025 (143) held close to the prior two-year average of 174.
Related Entities for Intraocular Pressure Lowering Implant
Top Manufacturers
Event Locations
Nationwide devices with a comparable report-volume footprint
Intraocular Pressure Lowering Implant carries zero death-typed MAUDE reports, so the peer set below compares report volume only; both axes are floored at ≥100 reports so the neighborhood stays in the advertised mass.
Similar report volume
Nearest other device types by FDA MAUDE report count (2,671 here).
Similar death-typed counts
Nearest other device types by death-typed report count (0 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Intraocular Pressure Lowering Implant are informational only and are not clinical advice. Report codes do not prove device causation. Consult a qualified clinician before acting on this data.
Every figure on PlainHospital is rendered directly from federal source data, no number is typed in by an editor. Event-type mix on this page is computed from FDA MAUDE codes for Intraocular Pressure Lowering Implant; corpus means use device types with ≥100 reports. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.