National Advanced Endoscopy Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
National Advanced Endoscopy Devices, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
National Advanced Endoscopy Devices, Inc. has 8 FDA 510(k) cleared medical devices. Based in Canoga Park, US.
Historical record: 8 cleared submissions from 1999 to 2017.
Browse the FDA 510(k) cleared devices submitted by National Advanced Endoscopy Devices, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - National Advanced Endoscopy Devices, Inc.
8 devices
Cleared
Aug 01, 2017
AED Sinuscope
Ear, Nose, Throat
183d
Cleared
Jan 07, 2015
AED HYSTEROSCOPE AND ACCESSORIES
Obstetrics & Gynecology
212d
Cleared
Dec 30, 2010
AED RESECTOSCOPE
Gastroenterology & Urology
106d
Cleared
Sep 29, 2008
AED BIPOLAR FORCEPS, MODEL 13-1646
General & Plastic Surgery
118d
Cleared
Sep 25, 2008
AED MONOPOLAR LAP ACCESSORIES
General & Plastic Surgery
119d
Cleared
Dec 15, 1999
AED CYSTOSCOPE
Gastroenterology & Urology
44d
Cleared
Dec 06, 1999
AED LAPAROSCOPE
General & Plastic Surgery
35d
Cleared
Dec 02, 1999
AED ARTHROSCOPE
Orthopedic
203d