Nanovis, LLC
Nanovis, LLC appears in FDA public data with 0 recalls, 10 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Sep 5, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K241605 | Adaptix PEEK Interbody System with Nanotechnology; Capstone Control PEEK Spinal System with Nanote | Sep 5, 2024 |
| K230936 | Anatomic PEEK Cervical Fusion System with Nanotechnology | Jun 2, 2023 |
| K203452 | Nano FortiFix® System | Dec 22, 2020 |
| K191822 | Nano FortiCore, FortiCore | Oct 11, 2019 |
| K171312 | FortiCore® | Jan 22, 2018 |
| K161485 | Nanovis Intervertebral Body Fusion System and Forticore(R) | Sep 6, 2016 |
| K160874 | Nanovis Intervertebral Body Fusion System and FortiCore® | Jun 28, 2016 |
| K140280 | FORTICORE | Sep 5, 2014 |
| K113173 | NANOVIS SPINAL SYSTEM | Jan 19, 2012 |
| K110442 | NANOVIS INTERVERTEBRAL BODY FUSION SYSTEM | Nov 9, 2011 |