510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K954128Substantially Equivalent

Snoremaster

D.D.S., Inc., Half Moon Bay CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K954128 is the FDA 510(k) clearance record for SNOREMASTER, a class II device, cleared for D.D.S., Inc. on under FDA product code LRK (Device, Anti-Snoring). FDA records list one 510(k) clearance for D.D.S., Inc. As of , FDA records show no recalls naming K954128.

Clearance record

Decision date
Received
(31 days to decision)
Product code
LRK Device, Anti-Snoring
Regulation
21 CFR 872.5570
Device class
Class II
Review panel
Dental
Applicant
D.D.S., Inc. 2181 St. Andrews Rd., Half Moon Bay CA
510(k) summary
Summary
Third party review
No

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