510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K963591Substantially Equivalent

Snoring Control Device

Kenneth Hilsen, New York NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K963591 is the FDA 510(k) clearance record for SNORING CONTROL DEVICE, a class II device, cleared for Kenneth Hilsen on under FDA product code LRK (Device, Anti-Snoring). FDA records list one 510(k) clearance for Kenneth Hilsen. As of , FDA records show no recalls naming K963591.

Clearance record

Decision date
Received
(487 days to decision)
Product code
LRK Device, Anti-Snoring
Regulation
21 CFR 872.5570
Device class
Class II
Review panel
Dental
Applicant
Kenneth Hilsen 12 E. 41st St., New York NY
510(k) summary
Statement
Third party review
No

Clearances, product code LRK

Trailing 12 months
14 clearances under product code LRK in the twelve months to October 2026, November 2025 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code LRK, trailing twelve months
MonthClearances
November 20253
December 20252
January 20260
February 20260
March 20262
April 20261
May 20261
June 20262
July 20261
August 20261
September 20260
October 20261