Product code KYF— Ophthalmic
AHMED GLAUCOMA VALVE IMPLANT
- Advisory panel
- Ophthalmic
- Total cleared
- 25
Adverse events under product code KYF
product code KYF- Injury
- 1,543
- Malfunction
- 646
- Total
- 2,189
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code KYF
- K230975 — Ahmed® Glaucoma Valve Model FP7
- K231051 — Ahmed® Glaucoma Valve Model FP8
- K220032 — iStent infinite Trabecular Micro-Bypass System, Model iS3
- K182518 — AHMED ClearPath Glaucoma Drainage Device
- K171451 — Ahmed Glaucoma Valve Model FP8
- K161457 — XEN Glaucoma Treatment System
- K162060 — Ahmed Glaucoma Valve
- K152996 — Molteno3 Glaucoma Implant
- K062252 — MOLTENO3
- K060644 — AHMED GLAUCOMA VALVE, MODEL M4
- K030350 — EXPRESS MINI GLAUCOMA SHUNT
- K012852 — EX-PRESS MINATURE GLAUCOMA IMPLANT, MODELS R-20, R-30, R-50, STS VERSIONS
- K991072 — AHMED GLAUCOMA VALVE IMPLANT
- K980657 — AHMED GLAUCOMA VALVE, MODEL S3
- K955455 — BAERVELT PARS PLANA GLAUCOMA IMPLANT
- K925636 — AHMED GLAUCOMA VALVE IMPLANT
- K905703 — KRUPIN EYE VALVE WITH DISK
- K902296 — TRABECULO-SUPRACHOROIDAL SHUNT
- K905129 — BAERVELDT GLAUCOMA IMPLANT
- K903462 — OPTIMED GLAUCOMA PRESSURE REGULATOR
- K902489 — MODIFIED MOLTENO(TM) IMPLANTS
- K890598 — MOLTENO IMPLANT
- K885125 — KRUPIN EYE VALVE W/SCLERAL BUCKLE
- K875099 — MOLTENO VALVE SETON
- K840204 — WHITE OCULAR PRESSURE RELIEF DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.