Monteris Medical, Inc. is one of 404 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Monteris Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NeuroBlate System, Monteris Medical NeuroBlate System, NeuroBlate System
8
Total
8
Cleared
0
Denied
Monteris Medical, Inc. has 8 FDA 510(k) cleared medical devices. Based in Winnipeg, Mb, CA.
Historical record: 8 cleared submissions from 2011 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Monteris Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Coombs Medical Device Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Monteris Medical, Inc.
8 devices
Cleared
Aug 21, 2020
NeuroBlate System
Neurology
122d
Cleared
Jul 25, 2017
Monteris Medical NeuroBlate System
General & Plastic Surgery
88d
Cleared
Oct 26, 2016
NeuroBlate System
General & Plastic Surgery
26d
Cleared
Feb 19, 2015
NeuroBlate System
General & Plastic Surgery
78d
Cleared
Jul 30, 2013
NEUROBLATE(TM) SYSTEM
General & Plastic Surgery
33d
Cleared
Jul 11, 2013
MONTERIS MEDICAL NEUROBLATE SYSTEM
General & Plastic Surgery
66d
Cleared
Apr 01, 2013
NEUROBLATE SYSTEM
General & Plastic Surgery
402d
Cleared
Apr 08, 2011
ATAMA SYSTEM
Radiology
53d