510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K963063Substantially Equivalent

Snore Tec

Marketing Technologies, Inc., Bakersfield CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K963063 is the FDA 510(k) clearance record for SNORE TEC, a class II device, cleared for Marketing Technologies, Inc. on under FDA product code LRK (Device, Anti-Snoring). FDA records list one 510(k) clearance for Marketing Technologies, Inc. As of , FDA records show no recalls naming K963063.

Clearance record

Decision date
Received
(250 days to decision)
Product code
LRK Device, Anti-Snoring
Regulation
21 CFR 872.5570
Device class
Class II
Review panel
Dental
Applicant
Marketing Technologies, Inc. 4000 Stockdale Hwy., Suite H, Bakersfield CA
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