Vision Quest Industries, Inc.
Irvine, CA, US
Vision Quest Industries, Inc. appears in FDA device records in Irvine, CA. FDA records list 6 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 6
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 6 510(k) clearances for Vision Quest Industries, Inc. between 1998 and 2015. The busiest year on record is 1998, with 1. The most recent is 2015, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1998 | 1 |
| 2003 | 1 |
| 2004 | 1 |
| 2008 | 1 |
| 2009 | 1 |
| 2015 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K142236 | BioniCare Hand System | NYN | Substantially Equivalent | |
| K090532 | T.E.A.R. TECH3 | IPF | Substantially Equivalent | |
| K072799 | TARGET STERILE ELECTRODE | GXY | Substantially Equivalent | |
| K041092 | FAST START TENS, MODEL FS 3001 | GZJ | Substantially Equivalent | |
| K030507 | T.E.A.R. TECH3 MODEL #44TT03 | IPF | Substantially Equivalent | |
| K982388 | SURGI STIM | IPF | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain