510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830042Substantially Equivalent

E-Z Jector

Innovators, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830042 is the FDA 510(k) clearance record for E-Z JECTOR, a class II device, cleared for Innovators, Inc. on under FDA product code EJI (Syringe, Cartridge). FDA records list 6 510(k) clearances for Innovators, Inc., from to . As of , FDA records show no recalls naming K830042.

Clearance record

Decision date
Received
(19 days to decision)
Product code
EJI Syringe, Cartridge
Regulation
21 CFR 872.6770
Device class
Class II
Review panel
Dental
Applicant
Innovators, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EJI

Trailing 12 months

FDA records hold no clearances under product code EJI in the trailing twelve months.

FDA records show no clearances under product code EJI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EJI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260