FHC, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
FHC, Inc. - FDA 510(k) Cleared Devices
Recent clearances: STarFix Designer Software C0265, VFS1 Bipolar Electrosurgical Generator, microTargeting Guideline 4000 5.0 System
12
Total
12
Cleared
0
Denied
FHC, Inc. has 12 FDA 510(k) cleared neurology devices. Based in Bowdoinham, US.
Last cleared in 2023. 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.
510(k) submissions have been managed by C2c Development, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - FHC, Inc.
12 devices
Cleared
Sep 08, 2023
STarFix Designer Software C0265
Neurology
140d
Cleared
May 14, 2020
VFS1 Bipolar Electrosurgical Generator
General & Plastic Surgery
112d
Cleared
Dec 20, 2018
microTargeting Guideline 4000 5.0 System
Neurology
37d
Cleared
Jul 26, 2012
MICROTARGETING XL STAR DRIVE SYSTEM
Neurology
23d
Cleared
Feb 12, 2010
WAYPOINT STEREOTACTIC SYSTEM
Neurology
206d
Cleared
Sep 18, 2009
MICROTARGETING STAR DRIVE SYSTEM, COMPONENTS
Neurology
29d
Cleared
Jul 25, 2007
MICROTARGETING GUIDELINE 4000
Neurology
70d
Cleared
Mar 24, 2004
MICRO TARGETING ELECTRODE
Neurology
175d
Cleared
Aug 30, 2001
MICRO TARGETING DRIVE SYSTEM
Neurology
84d
Cleared
Aug 14, 2001
FHC MICROTARGETING DRIVE SYSTEM
Neurology
49d
Cleared
Feb 23, 2001
MICROTARGETING DRIVE SYSTEM
Neurology
78d
Cleared
Aug 04, 2000
MICROTARGETING ELECTRODE
Neurology
459d