Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K032361Substantially Equivalent

Endopure Root Canal Cleanser

Dentsply Intl., York PA / Traditional, Substantially Equivalent

K032361 is the FDA 510(k) clearance record for ENDOPURE ROOT CANAL CLEANSER, cleared for Dentsply Intl. on under FDA product code KJJ (Cleanser, Root Canal). FDA records list 291 510(k) clearances for Dentsply Intl., from to . As of , FDA records show no recalls naming K032361.

Clearance record

Decision date
Received
(165 days to decision)
Product code
KJJ Cleanser, Root Canal
Device class
Unclassified
Review panel
Unknown
Applicant
Dentsply Intl. 570 W. College Ave., York PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KJJ

Trailing 12 months

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

FDA records show no clearances under product code KJJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KJJ, 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