Integrated Endoscopy, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242606 | Nuvis® Wireless HD Camera System (Nuvis-2K) | November 20, 2025 |
| K191594 | Nuvis Battery Arthroscope | July 11, 2019 |
| K140903 | NUVIS ARTHROSCOPE | July 17, 2014 |