Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Nanovis with 10 510(k) clearances. The most recent is a 510(k) clearance dated Sep 5, 2024: Adaptix™ PEEK Interbody System with Nanotechnology; Capstone Control™ PEEK Spinal System….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 5, 2024 | Adaptix™ PEEK Interbody System with Nanotechnology; Capstone Control™ PEEK Spinal System with NanotechnologyK241605 · MAX | 510(k) clearances |
| Jun 2, 2023 | Anatomic PEEK™ Cervical Fusion System with NanotechnologyK230936 · ODP | 510(k) clearances |
| Dec 22, 2020 | Nano FortiFix® SystemK203452 · NKB | 510(k) clearances |
| Oct 11, 2019 | Nano FortiCore, FortiCoreK191822 · ODP | 510(k) clearances |
| Jan 22, 2018 | FortiCore®K171312 · MAX | 510(k) clearances |
| Sep 6, 2016 | Nanovis Intervertebral Body Fusion System and Forticore(R)K161485 · MAX | 510(k) clearances |
| Jun 28, 2016 | Nanovis Intervertebral Body Fusion System and FortiCore®K160874 · MAX | 510(k) clearances |
| Sep 5, 2014 | FORTICOREK140280 · ODP | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
