Waismed Ltd.
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| Brand Name: NIO-A Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 105000 recall (Z-2118-2025) | Waismed Ltd. | 2025-07-17 |
| Brand Name: NIO+ Product Name: NIO Intraosseous Device Adult Model/Catalog Number: 1050009 recall (Z-2119-2025) | Waismed Ltd. | 2025-07-17 |
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Every clearance here is in the API, with alerts when new ones post.