Concentric Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Concentric Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever), Trevo XP ProVue Retriever (4x30mm), Trevo XP ProVue Retriever (6X25mm)
45
Total
44
Cleared
1
Denied
Concentric Medical, Inc. has 44 FDA 510(k) cleared medical devices. Based in Moutian View, US.
Historical record: 44 cleared submissions from 2001 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Concentric Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant. 5 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Concentric Medical, Inc.
45 devices
Cleared
CT
Feb 15, 2018
Trevo Pro Vue Retriever and Trevo XP Pro Vue Retriever (Trevo Retriever)
Neurology
113d
Not Cleared
Sep 02, 2016
Modified Trevo ProVue Retriever, Trevo XP ProVue Retriever 4x20mm, Trevo XP...
Neurology
312d
Cleared
Jun 12, 2015
Trevo XP ProVue Retriever (4x30mm)
Neurology
94d
Cleared
Apr 06, 2015
Trevo XP ProVue Retriever (6X25mm)
Neurology
161d
Cleared
CT
Feb 25, 2014
MODIFIED HD GUIDE CATHETER
Cardiovascular
131d
Cleared
CT
Jan 17, 2014
MODIFIED TREVO PROVUE RETRIEVER
Neurology
66d
Cleared
Jan 13, 2014
MODIFIED TREVO PROVUE RETRIEVER
Neurology
140d
Cleared
Oct 11, 2013
MODIFIED CONCENTRIC MICROCATHETER
Cardiovascular
144d
Cleared
CT
Oct 03, 2013
MODIFIED FLOWGATE BALLOON GUIDE CATHETER
Cardiovascular
133d
Cleared
Nov 21, 2012
MODIFIED BALLOON GUIDE CATHETER MODEL 90253, 90254
Cardiovascular
90d
Cleared
Oct 31, 2012
MODIFIED TREVO RETRIEVER
Neurology
78d
Cleared
CT
Aug 03, 2012
TREVO RETRIEVER
Neurology
126d
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