Integra Radionics, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Integra Radionics, Inc. has 10 FDA 510(k) cleared medical devices. Based in Burlington, US.
Historical record: 10 cleared submissions from 2006 to 2011. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Integra Radionics, Inc. Filter by specialty or product code using the sidebar.
10 devices
Cleared
Jun 10, 2011
CUSA NXT EXTENDED LENGTH TIP
General & Plastic Surgery
304d
Cleared
Apr 22, 2010
LINAC COLLIMATOR ASSEMBLY HOUSING (LCAH) MODEL LCAHART
Radiology
99d
Cleared
Apr 08, 2010
XKNIFE 5
Radiology
51d
Cleared
May 08, 2009
CUSA SHEAR TIP, AN ACCESSORY OF THE CUSA EXCEL ULTRASONIC SURGICAL ASPIRATOR...
General & Plastic Surgery
39d
Cleared
Mar 02, 2009
RADIONICS XKNIFE HDRT SYSTEM
Radiology
104d
Cleared
Aug 13, 2008
CUSA SELECTOR NXT ULTRASONIC TISSUE ABLATION SYSTEM
General & Plastic Surgery
82d
Cleared
Oct 16, 2007
INTEGRA RADIONICS INTERFIX PATIENT ADAPTERS
Radiology
46d
Cleared
Aug 17, 2007
INTEGRA SELECTOR ULTRASONIC SURGICAL ASPIRATOR SYSTEM WITH BONE TIP
General & Plastic Surgery
59d
Cleared
Dec 21, 2006
INTEGRA RADIONICS IMAGEFUSION 3
Radiology
57d
Cleared
Jul 25, 2006
INTEGRA RADIONICS XKNIFE RT 4
Radiology
22d