Dfine, Inc.
5 FDA 510(k) clearances · Manufacturer
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| ABLATION INSTRUMENT, MODEL 1635; ABLATION MULTIPLEX CATHETER, MODEL 1682 (K091310) | Dfine, Inc. | 2010-08-11 |
| STABILI ERX BONE CEMENT, MODEL 1135,STABILIT VERTEBRAL AUGMENTATION SYSTEM (FOR USE W/ STABILIT ERX BONE CEMENT) (K090986) | Dfine, Inc. | 2009-12-30 |
| MODIFICATION TO SPACE CPSXL BONE CEMENT (K072496) | Dfine, Inc. | 2007-10-05 |
| SPACE 360 DELIVERY SYSTEM (K070351) | Dfine, Inc. | 2007-06-29 |
| SPACE CPSXL BONE CEMENT (K061531) | Dfine, Inc. | 2006-08-30 |
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Every clearance here is in the API, with alerts when new ones post.