510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K133016Substantially Equivalent

Vent-Os Sinus Dilation System

Sinusys Corporation, Orinda CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K133016 is the FDA 510(k) clearance record for VENT-OS SINUS DILATION SYSTEM, a class I device, cleared for Sinusys Corporation on under FDA product code LRC (Instrument, Ent Manual Surgical). FDA records list 2 510(k) clearances for Sinusys Corporation, from to . As of , FDA records show no recalls naming K133016.

Clearance record

Decision date
Received
(75 days to decision)
Product code
LRC Instrument, Ent Manual Surgical
Regulation
21 CFR 874.4420
Device class
Class I
Review panel
Ear, Nose, Throat
Applicant
Sinusys Corporation 8 Snowberry Ct., Orinda CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LRC

Trailing 12 months

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

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