HMD
Tianjin Huahong Technology Co., Ltd. · Model IA,30G · UDI-DI 00810011730458
10
510(k) clearances
250
Adverse events
1
Recalls
87
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-07-25 | Home Health US, Incorporated | Due to incorrect/lack of Unique Device Identifier (UDI) codes. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.