Moss Tubes, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Moss Tubes, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV
5
Total
5
Cleared
0
Denied
Moss Tubes, Inc. has 5 FDA 510(k) cleared medical devices. Based in Castleton On Hudson, US.
Historical record: 5 cleared submissions from 1999 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Moss Tubes, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Xeridiem Medical Devices as regulatory consultant.
FDA 510(k) Regulatory Record - Moss Tubes, Inc.
5 devices
Cleared
Jun 14, 2019
Moss Gastrostomy Tube, Moss Nasal Tube – Mark IV
Gastroenterology & Urology
113d
Cleared
Mar 22, 1999
MOSS GASTROSTOMY TUBE
Gastroenterology & Urology
42d
Cleared
Mar 17, 1999
MODIFICATION OF MOSS P.E.G. TRAY
Gastroenterology & Urology
77d
Cleared
Mar 02, 1999
MOSS TUBES, INC. NASAL TUBE - MARK IV
Gastroenterology & Urology
62d
Cleared
Feb 24, 1999
MOSS TUBES, INC, ALL SILICONE GASTROSTOMY TUBE
Gastroenterology & Urology
84d