510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K120665Substantially Equivalent

Invent Snoring Device

Ventus Medical, Inc., Hillsborough CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K120665 is the FDA 510(k) clearance record for INVENT SNORING DEVICE, a class I device, cleared for Ventus Medical, Inc. on under FDA product code LWF (Dilator, Nasal). FDA records list 5 510(k) clearances for Ventus Medical, Inc., from to . As of , FDA records show no recalls naming K120665.

Clearance record

Decision date
Received
(99 days to decision)
Product code
LWF Dilator, Nasal
Regulation
21 CFR 874.3900
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Ventus Medical, Inc. 1171 Barroilhet Dr., Hillsborough CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LWF

Trailing 12 months

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

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