Home › Tomore Medical (Shenzhen) Co., Ltd › TOMORE
TOMORE
Tomore Medical (Shenzhen) Co., Ltd · Model Lucid508 · UDI-DI 06976110831725
0
510(k) clearances
12
Adverse events
1
Recalls
90
Facilities
Description
Hearing Aid
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-04-25 | HANGZHOU ACOSOUND TECHNOLOGY CO., LTD. | Three issues 1. Label error: The manufacturer information in the labeling is not correct, the manufacturer's name is mislabeled as "Developed by AcoSound," Correct should be "Manu |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.