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
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 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 6 |
| December 2025 | 6 |
| January 2026 | 4 |
| February 2026 | 1 |
| March 2026 | 6 |
| April 2026 | 3 |
| May 2026 | 11 |
| June 2026 | 3 |
| July 2026 | 6 |
| August 2026 | 3 |
| September 2026 | 3 |
| October 2026 | 0 |
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