Product code HNJ— Ophthalmic

DORC CORNEAL PUNCH BLOCK

Classification name
Punch, Corneo-Scleral
Device class
Class 1
Regulation
21 CFR 886.4350
Advisory panel
Ophthalmic
Total cleared
3
First cleared
Most recent

Market context for product code HNJ

FDA has cleared 3 devices under product code HNJ between 1979 and 1987, filed by 3 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 HNJ

Recent clearances under product code HNJ

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