Spineart SA
12 FDA 510(k) clearances · Manufacturer
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| SPINEART Navigation Instrument System (K261205) | Spineart SA | 2026-07-29 |
| PERLA® TL Posterior Thoraco-lumbar Fixation System (K253966) | Spineart SA | 2026-05-01 |
| SPINEART Navigation Instrument System (K254158) | Spineart SA | 2026-04-09 |
| SPINEART Navigation Instrument System (K242933) | Spineart SA | 2025-06-18 |
| SPINEART Navigation Instrument System (K242890) | Spineart SA | 2025-03-07 |
| Scarlet® AL-T (K242589) | Spineart SA | 2024-10-23 |
| SPINEART Navigation Instrument System (K241644) | Spineart SA | 2024-08-07 |
| Juliet® Ti LL Lumbar Interbody Device (K241321) | Spineart SA | 2024-07-18 |
| SCARLET® AC-Ti (K240699) | Spineart SA | 2024-05-10 |
| PERLA® TL Posterior Thoraco-lumbar Fixation System (K231069) | Spineart SA | 2023-10-25 |
| Tryptik Ti (K230583) | Spineart SA | 2023-03-22 |
| SPINEART Navigation Instrument System (K183630) | Spineart SA | 2019-06-10 |
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Every clearance here is in the API, with alerts when new ones post.