510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K944084Substantially Equivalent

Jeneric/pentron P0wered Toothbrust

Jeneric/Pentron, Inc., Chicago IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K944084 is the FDA 510(k) clearance record for JENERIC/PENTRON P0WERED TOOTHBRUST, a class I device, cleared for Jeneric/Pentron, Inc. on under FDA product code JEQ (Toothbrush, Powered). FDA records list 78 510(k) clearances for Jeneric/Pentron, Inc., from to . As of , FDA records show no recalls naming K944084.

Clearance record

Decision date
Received
(120 days to decision)
Product code
JEQ Toothbrush, Powered
Regulation
21 CFR 872.6865
Device class
Class I
Review panel
Dental
Applicant
Jeneric/Pentron, Inc. 1819 So. May St., Chicago IL
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