Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K223920Substantially Equivalent

Vinno G50, Vinno G55, Vinno M50, Vinno E30, Vinno X5, Vinno X6, Vinno X7, Vinno M55, Vinno E35, Vinno X65, Vinno X55, Vinno X35, Vinno G55e, Vinno G55p, Vinno M55e, Vinno M55p, Vinno E35e, Vinno E35p

Vinno Technology (Suzhou) Co.,Ltd, Suzhou, CN / Traditional, Substantially Equivalent

K223920 is the FDA 510(k) clearance record for VINNO G50, VINNO G55, VINNO M50, VINNO E30, VINNO X5, VINNO X6, VINNO X7, VINNO M55, VINNO E35, VINNO X65, VINNO X55, VINNO X35, VINNO G55E, VINNO G55P, VINNO M55E, VINNO M55P, VINNO E35E, VINNO E35P, a class II device, cleared for Vinno Technology (Suzhou) Co.,Ltd on under FDA product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic). FDA records list 6 510(k) clearances for Vinno Technology (Suzhou) Co.,Ltd, from to . As of , FDA records show no recalls naming K223920.

Clearance record

Decision date
Received
(170 days to decision)
Product code
IYN System, Imaging, Pulsed Doppler, Ultrasonic
Regulation
21 CFR 892.1550
Device class
Class II
Review panel
Radiology
Applicant
Vinno Technology (Suzhou) Co.,Ltd 5f Bldg. A, 4f Bldg. C # 27 Xinfa Rd., Suzhou, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IYN

Trailing 12 months
52 clearances under product code IYN in the twelve months to October 2026, May 2026 the highest month at 11.
Show the numbers
Monthly 510(k) clearances under FDA product code IYN, trailing twelve months
MonthClearances
November 20256
December 20256
January 20264
February 20261
March 20266
April 20263
May 202611
June 20263
July 20266
August 20263
September 20263
October 20260