Instradent USA, Inc.
2 FDA 510(k) clearances · Recalling firm
| Record | Firm | Date |
|---|---|---|
| NEODENT CM Intraoral Scanbody, Article Number: 108.139 recall (Z-1831-2017) | Instradent USA, Inc. | 2017-04-07 |
| Neodent Titamax WS Cortical Implant 4.0 x 5 mm (Endosseous dental implant) Article Number: recall (Z-0839-2015) | Instradent USA, Inc. | 2014-12-22 |
Track Instradent USA, Inc. automatically
Every clearance here is in the API, with alerts when new ones post.