Orthomerica Products, Inc. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Orthomerica Products, Inc. has 21 FDA 510(k) cleared neurology devices. Based in Washington, US.
Latest FDA clearance: Mar 2024. Active since 2000.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
21 devices
Cleared
Mar 15, 2024
STARband 3D
Neurology
28d
Cleared
Apr 20, 2023
STARband 3D
Neurology
182d
Cleared
Aug 17, 2021
STARband
Neurology
105d
Cleared
Apr 27, 2021
STARband, STARlight, St. Louis Band
Neurology
195d
Cleared
Mar 01, 2018
STARband, STARlight, St. Louis Band
Neurology
44d
Cleared
Jul 20, 2016
St. Louis Band
Neurology
89d
Cleared
Sep 18, 2015
STARband, STARlight
Neurology
63d
Cleared
Jul 01, 2015
STARband, STARlight
Neurology
62d
Cleared
Apr 23, 2015
STARBAND, STARLIGHT
Neurology
261d
Cleared
Oct 06, 2014
STARBAND, STARLIGHT
Neurology
90d
Cleared
Jun 06, 2014
STARBAND AND STARLIGHT
Neurology
114d
Cleared
Jan 16, 2014
STARLIGHT
Neurology
86d
Cleared
Jun 10, 2013
STARBAND
Neurology
164d
Cleared
Jul 17, 2009
STARLIGHT
Neurology
135d
Cleared
Dec 05, 2008
STARBAND
Neurology
63d
Cleared
Oct 31, 2008
STARLIGHT
Neurology
29d
Cleared
Sep 12, 2008
STARLIGHT
Neurology
60d
Cleared
Jul 25, 2002
CLARREN HELMET (ORTHOMERICA)
Neurology
44d
Cleared
Jul 09, 2002
STARLIGHT
Neurology
84d
Cleared
Jul 03, 2001
STARBAND CRANIAL ORTHOSIS
Neurology
62d
Cleared
Jul 07, 2000
OPI BAND
Neurology
88d