Home › Genabio Diagnostics Inc. › GenaCheck® COVID-19 Rapid Self-Test 2T
GenaCheck® COVID-19 Rapid Self-Test 2T
Genabio Diagnostics Inc. · Model N/A · UDI-DI 00810143620122
10
510(k) clearances
138
Adverse events
3
Recalls
24
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-06-26 | FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO.,LTD | The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States. |
| 2024-06-26 | FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO.,LTD | The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States. |
| 2024-06-26 | FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO.,LTD | The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States. |
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.
