510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K840459Substantially Equivalent

Improved Mouthpiece

Kinetix, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K840459 is the FDA 510(k) clearance record for IMPROVED MOUTHPIECE, a class I device, cleared for Kinetix on under FDA product code BYP (Mouthpiece, Breathing). FDA records list 4 510(k) clearances for Kinetix, from to . As of , FDA records show no recalls naming K840459.

Clearance record

Decision date
Received
(15 days to decision)
Product code
BYP Mouthpiece, Breathing
Regulation
21 CFR 868.5620
Device class
Class I
Review panel
Anesthesiology
Applicant
Kinetix 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code BYP

Trailing 12 months

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

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