Toray Industries (America), Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Toray Industries (America), Inc. - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Toray Industries (America), Inc. has 18 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 18 cleared submissions from 1986 to 2004. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Toray Industries (America), Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Toray Industries (America), Inc.
18 devices
Cleared
Dec 17, 2004
TORAYGUIDE GUIDEWIRE
Cardiovascular
108d
Cleared
Sep 29, 2003
TORAYSULFONE DIALYZER, BS-L SERIES
Gastroenterology & Urology
266d
Cleared
Oct 15, 2001
TORAYSULFONE DIALYZER
Gastroenterology & Urology
426d
Cleared
Aug 25, 2000
HEMOFEEL-CH, MODELS CH-0.35L, CH-0.6L, CH-1.0L
Gastroenterology & Urology
256d
Cleared
Jun 22, 1995
FILTRYZER
Gastroenterology & Urology
380d
Cleared
May 19, 1995
FILTRYZER(TM)
Gastroenterology & Urology
550d
Cleared
May 04, 1995
FILTRYZER
Gastroenterology & Urology
433d
Cleared
Mar 17, 1989
TORAY FILTRYZER DIALYZERS
Gastroenterology & Urology
154d
Cleared
Feb 27, 1989
TORAY FILTRYZER BK SERIES
Gastroenterology & Urology
200d
Cleared
Jan 12, 1989
TORAY VASCULAR PROSTHESIS
Cardiovascular
107d
Cleared
Aug 12, 1988
MODIFIED TORAY FILTRYZER DIALYZERS
Gastroenterology & Urology
81d
Cleared
May 11, 1988
TORAY ANTHRON P-U CATHETERS
General Hospital
50d
Cleared
Mar 07, 1988
TORAY SUPERSELECTIVE GUIDEWIRES, ADDITIONAL TYPES
Cardiovascular
125d
Cleared
Nov 20, 1987
TORAY ANTHRON ANGIOGRAPHIC CATHETERS
Cardiovascular
112d
Cleared
Sep 24, 1987
TORAY ANTHRON AORTA BYPASS TUBES
Cardiovascular
73d
Cleared
Jul 11, 1986
TORAY SUPERSELECTIVE GUIDEWIRE,SUPERSELEC Y-K TYPE
Cardiovascular
108d
Cleared
Jun 18, 1986
ANTHRON CATHETERS & SETS
General Hospital
85d
Cleared
May 28, 1986
TORAY ANTHRON BYPASS TUBES
Cardiovascular
64d