Nvision Biomedical Technologies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nvision Biomedical Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: VERTEX Nitinol Staple System, Vector Hammertoe Correction System, Healix™ Compression Screw System
10
Total
10
Cleared
0
Denied
Nvision Biomedical Technologies, LLC has 10 FDA 510(k) cleared orthopedic devices. Based in San Antonio, US.
Historical record: 10 cleared submissions from 2014 to 2019.
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 Watershed Ideas Foundry, Acknowledge Regulatory Strategies, LLC and Watershed Idea Foundry.
FDA 510(k) Regulatory Record - Nvision Biomedical Technologies, LLC
10 devices
Cleared
Apr 04, 2019
VERTEX Nitinol Staple System
Orthopedic
163d
Cleared
Feb 19, 2019
Vector Hammertoe Correction System
Orthopedic
109d
Cleared
Dec 04, 2018
Healix™ Compression Screw System
Orthopedic
42d
Cleared
Apr 17, 2018
FOCUS Pedicle Screw System
Orthopedic
56d
Cleared
Dec 06, 2017
Boundary Anterior Lumbar Buttress Plate
Orthopedic
68d
Cleared
Jan 24, 2017
nvc
Orthopedic
15d
Cleared
Sep 29, 2016
nva, nvp, and nvt
Orthopedic
30d
Cleared
Sep 02, 2016
Tangis Anterior Cervical Plate
Orthopedic
92d
Cleared
Dec 23, 2014
nvc
Orthopedic
125d
Cleared
Nov 28, 2014
nva, nvp, nvt
Orthopedic
74d