510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K933829Substantially Equivalent

Pulse Electric Toothbrush

Dentatech Corp., King City, Ontario, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933829 is the FDA 510(k) clearance record for PULSE ELECTRIC TOOTHBRUSH, a class I device, cleared for Dentatech Corp. on under FDA product code JEQ (Toothbrush, Powered). FDA records list one 510(k) clearance for Dentatech Corp. As of , FDA records show no recalls naming K933829.

Clearance record

Decision date
Received
(130 days to decision)
Product code
JEQ Toothbrush, Powered
Regulation
21 CFR 872.6865
Device class
Class I
Review panel
Dental
Applicant
Dentatech Corp. 15 Keele St. S., King City, Ontario, CA
510(k) summary
Statement
Third party review
No

Clearances, product code JEQ

Trailing 12 months

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

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