Product code HOX— Ophthalmic

'E' CUBE AND 'E' PAD

Classification name
Chart, Visual Acuity
Device class
Class 1
Regulation
21 CFR 886.1150
Advisory panel
Ophthalmic
Total cleared
32
First cleared
Most recent

Market context for product code HOX

FDA has cleared 32 devices under product code HOX between 1978 and 2010, filed by 22 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

Top applicants under product code HOX

Recent clearances under product code HOX

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