Nanovis, LLC

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241605Adaptix™ PEEK Interbody System with Nanotechnology; Capstone Control™ PEEK Spinal System with NanoteSeptember 5, 2024
K230936Anatomic PEEK™ Cervical Fusion System with NanotechnologyJune 2, 2023
K203452Nano FortiFix® SystemDecember 22, 2020
K191822Nano FortiCore, FortiCoreOctober 11, 2019
K171312FortiCore®January 22, 2018
K161485Nanovis Intervertebral Body Fusion System and Forticore(R)September 6, 2016
K160874Nanovis Intervertebral Body Fusion System and FortiCore®June 28, 2016
K140280FORTICORESeptember 5, 2014
K113173NANOVIS SPINAL SYSTEMJanuary 19, 2012
K110442NANOVIS INTERVERTEBRAL BODY FUSION SYSTEMNovember 9, 2011