Cedic S.R.L. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Cedic S.R.L. - FDA 510(k) Cleared Devices
Recent clearances: Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes, ENConnect 40 mm Screw Cap to ENPlus Adapter
7
Total
7
Cleared
0
Denied
Cedic S.R.L. has 7 FDA 510(k) cleared medical devices. Based in Peschiera Borromeo, IT.
Historical record: 7 cleared submissions from 2005 to 2019. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Cedic S.R.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Koelper Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cedic S.R.L.
7 devices
Cleared
Apr 25, 2019
Cediflo Enteral Feeding Tubes & Cediflo Junior Enteral Feeding Tubes
Gastroenterology & Urology
294d
Cleared
Apr 09, 2019
ENConnect 40 mm Screw Cap to ENPlus Adapter
Gastroenterology & Urology
55d
Cleared
May 04, 2017
Cedic Enteral ENFit Transition Connectors
Gastroenterology & Urology
267d
Cleared
Apr 02, 2015
Cedic Oral/Luer Enteral ENFit Transition Connector for Medication Port
Gastroenterology & Urology
90d
Cleared
Oct 17, 2014
CEDIC ENTERAL DISTAL END ENFIT TRANSITION CONNECTOR, CEDIC ENTERAL ENFIT...
Gastroenterology & Urology
225d
Cleared
Jan 18, 2008
ENTERAL FEEDING SPIKE ADAPTER
Gastroenterology & Urology
120d
Cleared
Jan 27, 2005
F00010 - IV GRAVITY SETWITH MALE LUER SLIP
General Hospital
174d