Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K230160Substantially Equivalent

Vinno G86,vinno G86e,vinno G65,vinno G65p,vinno G65e,vinno G65d,vinno M86, Vinno M86e,vinno G90,vinno G90e

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

K230160 is the FDA 510(k) clearance record for VINNO G86,VINNO G86E,VINNO G65,VINNO G65P,VINNO G65E,VINNO G65D,VINNO M86, VINNO M86E,VINNO G90,VINNO G90E, 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 K230160.

Clearance record

Decision date
Received
(155 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