Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Magic Mobility — Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K233877 | XT Series Power Wheelchair (XT2), XT Series Power Wheelchair | Magic Mobility | 2024-03-04 | 88 | 0 |
| K213090 | Frontier Series Power Wheelchairs | Magic Mobility | 2021-11-19 | 56 | 0 |
| K211574 | Extreme X8 | Magic Mobility | 2021-07-09 | 49 | 0 |
| K203083 | Magic 360 Power Wheelchair | Magic Mobility | 2021-03-17 | 155 | 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