Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K061689Substantially Equivalent

Aquatine Ec Endodontic Cleanser

Puricore, Inc., Radnor PA / Traditional, Substantially Equivalent

K061689 is the FDA 510(k) clearance record for AQUATINE EC ENDODONTIC CLEANSER, cleared for Puricore, Inc. on under FDA product code KJJ (Cleanser, Root Canal). FDA records list 10 510(k) clearances for Puricore, Inc., from to . As of , FDA records show no recalls naming K061689.

Clearance record

Decision date
Received
(70 days to decision)
Product code
KJJ Cleanser, Root Canal
Device class
Unclassified
Review panel
Unknown
Applicant
Puricore, Inc. 320 King Of Prussia Rd., Radnor 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