510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K262515Substantially Equivalent

Kneu Platform (V2)

Kneu Health Digital , Ltd., London, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K262515 is the FDA 510(k) clearance record for Kneu Platform (V2), a class II device, cleared for Kneu Health Digital , Ltd. on under FDA product code GYD (Transducer, Tremor). As of , FDA records show no recalls naming K262515.

Clearance record

Decision date
Received
(30 days to decision)
Product code
GYD Transducer, Tremor
Regulation
21 CFR 882.1950
Device class
Class II
Review panel
Neurology
Applicant
Kneu Health Digital , Ltd. Blackwell House, Guildhall Yard, London, GB
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code GYD

Trailing 12 months
3 clearances under product code GYD in the twelve months to October 2026, August 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code GYD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20262
September 20260
October 20260