Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K121165Substantially Equivalent

Beam Brush/beam App

Beam Technologies, LLC, Louisville KY / Traditional, Substantially Equivalent

K121165 is the FDA 510(k) clearance record for BEAM BRUSH/BEAM APP, a class I device, cleared for Beam Technologies, LLC on under FDA product code EFW (Toothbrush, Manual). FDA records list one 510(k) clearance for Beam Technologies, LLC. As of , FDA records show no recalls naming K121165.

Clearance record

Decision date
Received
(65 days to decision)
Product code
EFW Toothbrush, Manual
Regulation
21 CFR 872.6855
Device class
Class I
Review panel
Dental
Applicant
Beam Technologies, LLC P.O. Box 17541, Louisville KY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EFW

Trailing 12 months

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

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