510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
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K811175Substantially Equivalent

Recoh Root Canal Irrigator

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

K811175 is the FDA 510(k) clearance record for RECOH ROOT CANAL IRRIGATOR, a class I device, cleared for Koei International, Inc. on under FDA product code EFS (Unit, Oral Irrigation). FDA records list one 510(k) clearance for Koei International, Inc. As of , FDA records show no recalls naming K811175.

Clearance record

Decision date
Received
(29 days to decision)
Product code
EFS Unit, Oral Irrigation
Regulation
21 CFR 872.6510
Device class
Class I
Review panel
Dental
Applicant
Koei International, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code EFS

Trailing 12 months

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

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