Nanovis, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nanovis, LLC - FDA 510(k) Cleared Devices
Recent clearances: Adaptix™ PEEK Interbody System with Nanotechnology, Anatomic PEEK™ Cervical Fusion System with Nanotechnology, Nano FortiFix® System
10
Total
10
Cleared
0
Denied
Nanovis, LLC has 10 FDA 510(k) cleared orthopedic devices. Based in San Diego, US.
Latest FDA clearance: Sep 2024. Active since 2011.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Backroads Consulting, Inc. and Backroads Consulting.
FDA 510(k) Regulatory Record - Nanovis, LLC
10 devices
Cleared
Sep 05, 2024
Adaptix™ PEEK Interbody System with Nanotechnology
Orthopedic
93d
Cleared
Jun 02, 2023
Anatomic PEEK™ Cervical Fusion System with Nanotechnology
Orthopedic
60d
Cleared
Dec 22, 2020
Nano FortiFix® System
Orthopedic
29d
Cleared
Oct 11, 2019
Nano FortiCore, FortiCore
Orthopedic
95d
Cleared
Jan 22, 2018
FortiCore®
Orthopedic
263d
Cleared
Sep 06, 2016
Nanovis Intervertebral Body Fusion System and Forticore(R)
Orthopedic
98d
Cleared
Jun 28, 2016
Nanovis Intervertebral Body Fusion System and FortiCore®
Orthopedic
90d
Cleared
Sep 05, 2014
FORTICORE
Orthopedic
213d
Cleared
Jan 19, 2012
NANOVIS SPINAL SYSTEM
Orthopedic
84d
Cleared
Nov 09, 2011
NANOVIS INTERVERTEBRAL BODY FUSION SYSTEM
Orthopedic
266d