510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K911470Substantially Equivalent

Buffing Floss

Lamar Industries, Sacramento CA / Traditional, Substantially Equivalent

K911470 is the FDA 510(k) clearance record for BUFFING FLOSS, a class I device, cleared for Lamar Industries on under FDA product code JES (Floss, Dental). FDA records list one 510(k) clearance for Lamar Industries. As of , FDA records show no recalls naming K911470.

Clearance record

Decision date
Received
(42 days to decision)
Product code
JES Floss, Dental
Regulation
21 CFR 872.6390
Device class
Class I
Review panel
Dental
Applicant
Lamar Industries 645-2 Woodside Sierra, Sacramento CA
Third party review
No

Clearances, product code JES

Trailing 12 months

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

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