Zhejiang Innuovo Rehabilitation Devices Co.,Ltd

FDA Regulatory Profile

Zhejiang Innuovo Rehabilitation Devices Co.,Ltd appears in FDA public data with 0 recalls, 18 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 18, 2026.

Summary

Total Recalls
0
510(k) Clearances
18
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253812Power Wheelchair (W5915B, W5915C, W5915D)June 18, 2026
K260056Power Wheelchair (N5515A, N5516, N5517A, N5519)June 5, 2026
K253806Power Wheelchair (N5919 series)April 20, 2026
K242471Power Wheelchair (W5538)November 18, 2024
K242387Mobility Scooter (N3473)October 11, 2024
K240990Mobility ScooterSeptember 10, 2024
K240008Mobility Scooter (W3331)June 5, 2024
K240012Mobility Scooter (W3431)May 2, 2024
K230964Power Wheelchair (N5909)December 13, 2023
K231508Power Wheelchair, W5521November 9, 2023
K231428Mobility Scooter (Models: W3431D)July 14, 2023
K222507Mobility Scooter (Models: W3431Q, W3431R)February 28, 2023
K222495Mobility Scooter, Model: W3331FOctober 17, 2022
K221026Power WheelchairJuly 1, 2022
K220740Power Wheelchair, W5907 (Q50 R Carbon)May 12, 2022
K220747Power Wheelchair (N5515B)May 12, 2022
K220207Mobility Scooter, Model W3468March 24, 2022
K220206Mobility ScooterMarch 24, 2022