Vision Quest Industries, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Vision Quest Industries, Inc.” (first 1998, latest 2015), across 4 product codes in 2 review panels. Median 510(k) review time under this name: 148 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 | 1 | 222 |
| 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 |
|---|---|---|---|
| IPF | Stimulator, Muscle, Powered | 3 | 3 |
| GXY | Electrode, Cutaneous | 1 | 1 |
| GZJ | Stimulator, Nerve, Transcutaneous, For Pain Relief | 1 | 1 |
| NYN | Stimulator, Electrical, Transcutaneous, For Arthritis | 1 | 1 |
Review panels
- Neurology (3)
- Physical Medicine (3)
Most recent Vision Quest Industries, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K142236 | BioniCare Hand System | NYN | 2015-03-23 | 222 |
| K090532 | T.E.A.R. TECH3 | IPF | 2009-11-13 | 259 |
| K072799 | TARGET STERILE ELECTRODE | GXY | 2008-04-24 | 206 |
| K041092 | FAST START TENS, MODEL FS 3001 | GZJ | 2004-07-01 | 66 |
| K030507 | T.E.A.R. TECH3 MODEL #44TT03 | IPF | 2003-05-20 | 90 |
| K982388 | SURGI STIM | IPF | 1998-09-14 | 67 |
Recalls
openFDA lists no recalls under a recalling firm named Vision Quest Industries, Inc..
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.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Vision-Sciences, Inc. (33 510(k)s)
- Vision Rt, Ltd. (11 510(k)s)
- Vision Health Technology (3 510(k)s)
- Vision Biosystems, Inc. (2 510(k)s)
- Vision Electronics (2 510(k)s)
- Vision Medical, Inc. (2 510(k)s)
- Vision Quest Industries Inc./Dba VQ Orthocare (2 510(k)s)
- Vision Science Co., Ltd. (2 510(k)s)
- Vision Systems Group, A Division of Viking Systems (2 510(k)s)
- Vision Ten, Inc. (2 510(k)s)
- Vision Chips, Inc. (1 510(k)s)
- Vision Design Eyewear, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Vision Quest Industries, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Vision Quest Industries, Inc.” (first 1998, latest 2015), across 4 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Vision Quest Industries, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Vision Quest Industries, Inc. is 148 days.
Which FDA product codes appear under Vision Quest Industries, Inc.?
The most frequent FDA product codes under this applicant name are IPF (Stimulator, Muscle, Powered, 3); GXY (Electrode, Cutaneous, 1); GZJ (Stimulator, Nerve, Transcutaneous, For Pain Relief, 1).
Next steps
- See all 6 Vision Quest Industries, Inc. clearances with predicates and recalls
- Run predicate analysis for product code IPF, Vision Quest Industries, Inc.'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 (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.