Conmed Endoscopic Technologies, Inc. is one of 15061 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Conmed Endoscopic Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DEUCE POLYPECTOMY SNARE, MODELS 000995, 000996,000997, 000998, CONMED AXCESS PAPILLOTOME MODELS AX4535, AX4535FX
2
Total
2
Cleared
0
Denied
Conmed Endoscopic Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Billerica, US.
Historical record: 2 cleared submissions from 2008 to 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Conmed Endoscopic Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Conmed Endoscopic Technologies, Inc.
2 devices