Biospace Corporation Limited is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biospace Corporation Limited - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Biospace Corporation Limited has 9 FDA 510(k) cleared medical devices. Based in Deer Field, US.
Historical record: 9 cleared submissions from 2005 to 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Biospace Corporation Limited Filter by specialty or product code using the sidebar.
Biospace Corporation Limited — FDA 510(k) Products and Clearance History
9 devices
Cleared
Sep 23, 2014
BIOSPACE BODY COMPOSITION ANALYZER
Gastroenterology & Urology
110d
Cleared
Nov 25, 2013
INBODY
Gastroenterology & Urology
249d
Cleared
Sep 04, 2013
BIOSPACE
Cardiovascular
141d
Cleared
Mar 08, 2013
INBODY 770, INBODY 570, INBODY S10, INBODY H20/INBODY H20(B)
Gastroenterology & Urology
144d
Cleared
Aug 19, 2011
INBODY
Gastroenterology & Urology
157d
Cleared
Mar 10, 2010
INBODY, MODELS: 270, R20, R20B
Gastroenterology & Urology
181d
Cleared
Feb 15, 2007
BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230
Gastroenterology & Urology
167d
Cleared
Dec 16, 2005
BIOSPACE BODY COMPOSITION ANALYZERS, MODELS INBODY 520, 720 AND S20
Gastroenterology & Urology
81d
Cleared
Jan 11, 2005
INBODY, MODEL 3.0
Gastroenterology & Urology
116d