Shanghai Hubang Intelligent Rehabilitation Equipment Co.,Ltd

FDA Regulatory Profile

Shanghai Hubang Intelligent Rehabilitation Equipment Co.,Ltd appears in FDA public data with 0 recalls, 1 510(k) clearance, 1 FDA inspection, and 0 compliance actions on record. Its most recent FDA inspection ended on Sep 4, 2025 (Voluntary Action Indicated (VAI)). Its most recent 510(k) clearance was granted on May 31, 2024.

Reviewing Shanghai Hubang Intelligent Rehabilitation Equipment Co.,Ltd as a supplier? Get its full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.

Get a free API key

Summary

Total Recalls
0
510(k) Clearances
1
Inspections
1
Compliance Actions
0

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 4, 2025Shanghai, ChinaDevicesVoluntary Action Indicated (VAI)3030410174

FDA Data Dashboard classifications: NAI (no action indicated), VAI (voluntary action indicated), OAI (official action indicated).

Recent 510(k) Clearances

K-NumberDeviceDate
K240913Electric Wheelchair (HBLD3-B); Electric Wheelchair (HBLD3-E)May 31, 2024