DeviceClearance

Product code KYF— Ophthalmic

AHMED GLAUCOMA VALVE IMPLANT

Classification name
Implant, Eye Valve
Device class
Class 2
Regulation
21 CFR 886.3920
Advisory panel
Ophthalmic
Total cleared
25
First cleared
Most recent

Market context for product code KYF

FDA has cleared 25 devices under product code KYF between 1985 and 2023, filed by 13 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code KYF

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.