Orthosensor, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthosensor, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VERASENSE for Exactech Equinoxe Size 38 mm, VERASENSE for Exactech Equinoxe Size 42 mm, LinkStation MINI, LinkStation MINI Evaluation Kit, VERASENSE Software Application for Shoulder, VERASENSE for Stryker Triathlon, VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left, VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Right, VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Left, VERASENSE for Zimmer Biomet Persona CR E-F/3-11 Right, VERASENSE for Zimmer Biomet Persona CR G-H/7-12 Left
8
Total
8
Cleared
0
Denied
Orthosensor, Inc. has 8 FDA 510(k) cleared medical devices. Based in Appollo Beach, US.
Historical record: 8 cleared submissions from 2009 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthosensor, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Orthosensor, Inc.
8 devices
Cleared
Aug 25, 2020
VERASENSE for Exactech Equinoxe Size 38 mm, VERASENSE for Exactech Equinoxe...
Orthopedic
172d
Cleared
Apr 12, 2020
VERASENSE for Stryker Triathlon
Orthopedic
30d
Cleared
Apr 01, 2020
VERASENSE for Zimmer Biomet Persona CR C-D/3-9 Left, VERASENSE for Zimmer...
Orthopedic
100d
Cleared
Jun 07, 2018
VERASENSE for Zimmer Biomet Persona
Orthopedic
107d
Cleared
Apr 15, 2016
VERASENSE Knee System
Orthopedic
427d
Cleared
Nov 08, 2013
ORTHOSENSOR KNEE BALANCER, VERASENSE KNEE SYSTEM
Orthopedic
144d
Cleared
Jun 13, 2013
ORTHOSENSOR KNEE BALANCER
Orthopedic
119d
Cleared
Oct 19, 2009
ORTHOREX INTRA-OPERATIVE LOAD SENSOR
Orthopedic
237d