510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K880956Substantially Equivalent

Snoar(tm) Open Airway Appliance

Kent J. Toone, D.D.S., Cupertino CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K880956 is the FDA 510(k) clearance record for SNOAR(TM) OPEN AIRWAY APPLIANCE, a class II device, cleared for Kent J. Toone, D.D.S. on under FDA product code LQZ (Device, Jaw Repositioning). FDA records list one 510(k) clearance for Kent J. Toone, D.D.S. As of , FDA records show no recalls naming K880956.

Clearance record

Decision date
Received
(65 days to decision)
Product code
LQZ Device, Jaw Repositioning
Regulation
21 CFR 872.5570
Device class
Class II
Review panel
Dental
Applicant
Kent J. Toone, D.D.S. 10301 S. De Anza Blvd., Cupertino CA
Third party review
No

Clearances, product code LQZ

Trailing 12 months

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

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