510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K150941Substantially Equivalent

Somnowell Mandibular Advancement Appliance (MAA)

Somnowell, Ltd., London, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K150941 is the FDA 510(k) clearance record for Somnowell Mandibular Advancement Appliance (MAA), a class II device, cleared for Somnowell , Ltd. on under FDA product code LRK (Device, Anti-Snoring). FDA records list one 510(k) clearance for Somnowell , Ltd. As of , FDA records show no recalls naming K150941.

Clearance record

Decision date
Received
(44 days to decision)
Product code
LRK Device, Anti-Snoring
Regulation
21 CFR 872.5570
Device class
Class II
Review panel
Dental
Applicant
Somnowell , Ltd. Idease House, Station Estate, London, GB
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code LRK

Trailing 12 months
13 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 20260