Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Novoxel , Ltd. — Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K240512 | Tixel i (TXLI0001) | Novoxel , Ltd. | 2024-11-04 | 256 | 0 |
| K223033 | Tixel® 2 System | Novoxel , Ltd. | 2023-06-21 | 265 | 0 |
| K202988 | Tixel System | Novoxel , Ltd. | 2021-02-25 | 148 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda