Gynova, LLC
Gynova, LLC appears in FDA public data with 0 recalls, 1 510(k) clearance, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 6, 2006.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K052420 | G-SPEC ARTICULATED WEIGHTED VAGINAL SPECULUM | April 6, 2006 |