Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Vestil Manufacturing Corp. — Predicate Candidate Screening
6 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
58 daysmedian FDA review time
151 days90th percentile
6clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K090350 | EXTREME 4X4-X8 POWER WHEELCHAIR | Vestil Manufacturing Corp. | 2009-04-10 | 58 | 0 |
| K030783 | FRONTIER MODEL X5 | Vestil Manufacturing Corp. | 2003-04-04 | 23 | 0 |
| K021866 | KARMA 800 SERIES MANUAL WHEELCHAIR | Vestil Manufacturing Corp. | 2002-06-14 | 8 | 0 |
| K014127 | KARMA DISCOVERY, MODEL KP40 | Vestil Manufacturing Corp. | 2002-03-15 | 88 | 0 |
| K011374 | JEWEL MPS | Vestil Manufacturing Corp. | 2001-05-29 | 25 | 0 |
| K000796 | MAGIC MOBILITY 4 X 4 WHEELCHAIR | Vestil Manufacturing Corp. | 2000-08-11 | 151 | 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