Vestil Manufacturing Corp.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Vestil Manufacturing Corp.” (first 2000, latest 2009), across 2 product codes in 1 review panel. Median 510(k) review time under this name: 42 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| ITI | Wheelchair, Powered | 4 | 4 |
| IOR | Wheelchair, Mechanical | 2 | 2 |
Review panels
Most recent Vestil Manufacturing Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K090350 | EXTREME 4X4-X8 POWER WHEELCHAIR | ITI | 2009-04-10 | 58 |
| K030783 | FRONTIER MODEL X5 | ITI | 2003-04-04 | 23 |
| K021866 | KARMA 800 SERIES MANUAL WHEELCHAIR | IOR | 2002-06-14 | 8 |
| K014127 | KARMA DISCOVERY, MODEL KP40 | ITI | 2002-03-15 | 88 |
| K011374 | JEWEL MPS | IOR | 2001-05-29 | 25 |
| K000796 | MAGIC MOBILITY 4 X 4 WHEELCHAIR | ITI | 2000-08-11 | 151 |
Recalls
openFDA lists no recalls under a recalling firm named Vestil Manufacturing Corp..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Vestil Manufacturing Corp.?
FDA lists 6 510(k) clearances under the applicant name “Vestil Manufacturing Corp.” (first 2000, latest 2009), across 2 product codes in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Vestil Manufacturing Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Vestil Manufacturing Corp. is 42 days.
Which FDA product codes appear under Vestil Manufacturing Corp.?
The most frequent FDA product codes under this applicant name are ITI (Wheelchair, Powered, 4); IOR (Wheelchair, Mechanical, 2).
Next steps
- See all 6 Vestil Manufacturing Corp. clearances with predicates and recalls
- Run predicate analysis for product code ITI, Vestil Manufacturing Corp.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.