510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K900178Substantially Equivalent

Electric Motor W/physio Dispenser, Handpieces

Core-Vent Corp., Encino CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900178 is the FDA 510(k) clearance record for ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES, a class I device, cleared for Core-Vent Corp. on under FDA product code EFS (Unit, Oral Irrigation). FDA records list 25 510(k) clearances for Core-Vent Corp., from to . As of , FDA records show no recalls naming K900178.

Clearance record

Decision date
Received
(135 days to decision)
Product code
EFS Unit, Oral Irrigation
Regulation
21 CFR 872.6510
Device class
Class I
Review panel
Dental
Applicant
Core-Vent Corp. 15821 Ventura Blvd., Encino CA
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