Medicon EG - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Medicon EG has 17 FDA 510(k) cleared medical devices. Based in Black Diamond, US.
Historical record: 17 cleared submissions from 1995 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Medicon EG Filter by specialty or product code using the sidebar.
17 devices
Cleared
Mar 24, 2017
MEDICON Spinal Spreading Systems
Neurology
280d
Cleared
Dec 06, 2010
MEDICON MOGEN CLAMP
Obstetrics & Gynecology
248d
Cleared
Mar 10, 2010
FIXIT HEADREST CLAMP SYSTEM
Neurology
443d
Cleared
Jul 17, 2006
MEDICON STERN-A-FIX STERNAL CLOSURE SYSTEM
Orthopedic
201d
Cleared
Jun 15, 2005
MEDICON IMF-ORION SCREWS
Dental
111d
Cleared
Feb 23, 2005
MEDICON 2.4 MANDIBULAR RECONSTRUCTION PLATING SYSTEM
Dental
86d
Cleared
Jan 13, 2005
MEDICON VIPAIR HIGH SPEED SYSTEM
Neurology
77d
Cleared
Aug 19, 2004
AARHUS ANCHORAGE SYSTEM
Dental
72d
Cleared
Aug 01, 2001
MEDICON TITANIUM YASARGIL ANEURYSM CLIPS
Neurology
128d
Cleared
Aug 01, 2001
MEDICON YASARGIL CLIP APPLYING FORCEPS
Neurology
128d
Cleared
Jan 16, 1998
SERVOTRONIC EC100 SYSTEM
Neurology
168d
Cleared
Mar 11, 1997
INTRAORAL MANDIBULAR DISTRACTION DEVICE
Dental
47d
Cleared
Jul 27, 1995
MESH TITANIUM IMPLANT SYSTEM
Dental
113d
Cleared
Jul 27, 1995
TITANIUM MANDIBULAT RECONSTRUCTION SYSTEM
Dental
113d
Cleared
Jul 26, 1995
MICRO TITANIUM PLATE SYSTEM
Dental
112d
Cleared
Jul 26, 1995
TITANIUM MINIPLATE SYSTEM
Dental
112d
Cleared
Jul 26, 1995
CMS CRANIO MAXILLO FACIAL TITANIUM IMPLANT SYSTEM
Dental
112d