Product code HMX— Ophthalmic

CANNULAS

Classification name
Cannula, Ophthalmic
Device class
Class 1
Regulation
21 CFR 886.4350
Advisory panel
Ophthalmic
Total cleared
77
First cleared
Most recent

Market context for product code HMX

FDA has cleared 77 devices under product code HMX between 1977 and 2001, filed by 35 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

last 15 years

Top applicants under product code HMX

Adverse events under product code HMX

product code HMX
Other
1
Total
1

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 HMX

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