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