Integra Radionics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - Integra Radionics, Inc.
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