Product code EJI— Dental

ANESTHESIA INJECTION TOOL SET

Classification name
Syringe, Cartridge
Device class
Class 2
Regulation
21 CFR 872.6770
Advisory panel
Dental
Total cleared
45
First cleared
Most recent

Market context for product code EJI

FDA has cleared 45 devices under product code EJI between 1980 and 2017, filed by 42 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 EJI

Recent clearances under product code EJI

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