510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K811831Substantially Equivalent

Multi-Purpose Dental Syringe

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

K811831 is the FDA 510(k) clearance record for MULTI-PURPOSE DENTAL SYRINGE, a class II device, cleared for Centrix, Inc. on under FDA product code EJI (Syringe, Cartridge). FDA records list 47 510(k) clearances for Centrix, Inc., from to . As of , FDA records show no recalls naming K811831.

Clearance record

Decision date
Received
(71 days to decision)
Product code
EJI Syringe, Cartridge
Regulation
21 CFR 872.6770
Device class
Class II
Review panel
Dental
Applicant
Centrix, 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