Gynex Corporation
Gynex Corporation appears in FDA public data with 1 recall, 0 510(k) clearances, 7 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0008-2013, Class III) was initiated on September 6, 2012.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 0
- Inspections
- 7
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-0008-2013 | Class III | Sterile, single-use, disposable electrosurgical electrode holder. It connects the electrode to the | September 6, 2012 |