510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
DEN200017Unknown

Q-Collar

Q30 Sports Science, LLC, Westport CT / Direct, Unknown
FDA source (opens on fda.gov)

DEN200017 is the FDA 510(k) clearance record for Q-Collar, a class II device, cleared for Q30 Sports Science, LLC on under FDA product code QNX (External Compression Device For Internal Jugular Vein Compression). FDA's definition for product code QNX reads: "External compression device for internal jugular vein compression. An external compression device for internal jugular vein compression is a non-invasive device that is intended to increase intracranial blood volume to reduce the...". FDA records list one 510(k) clearance for Q30 Sports Science, LLC. As of , FDA records show no recalls naming DEN200017.

Clearance record

Decision date
Received
(344 days to decision)
Product code
QNX External Compression Device For Internal Jugular Vein Compression
Regulation
21 CFR 890.3050
Device class
Class II
Review panel
Neurology
Applicant
Q30 Sports Science, LLC 257 Riverside Ave., Westport CT
Third party review
No

Clearances, product code QNX

Trailing 12 months

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

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