510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K123538Substantially Equivalent

Epien Root Canal Cleanser

Epien Medical, Inc., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K123538 is the FDA 510(k) clearance record for EPIEN ROOT CANAL CLEANSER, cleared for Epien Medical, Inc. on under FDA product code KJJ (Cleanser, Root Canal). FDA records list 2 510(k) clearances for Epien Medical, Inc., from to . As of , FDA records show no recalls naming K123538.

Clearance record

Decision date
Received
(77 days to decision)
Product code
KJJ Cleanser, Root Canal
Device class
Unclassified
Review panel
Unknown
Applicant
Epien Medical, Inc. 700 Thirteenth St. NW Stuite 200, Washington DC
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