Medical Device Manufacturer · US , Baltimore , MD

Corindus, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2012

Recent clearances: CorPath GRX System, CorPath GRX System, CorPath GRX System

Total

Cleared

Denied

Corindus, Inc. has 9 FDA 510(k) cleared medical devices. Based in Baltimore, US.

Last cleared in 2022. Active since 2012. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Corindus, Inc. Filter by specialty or product code using the sidebar.

Corindus, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Corindus, Inc.

9 devices

1-9 of 9

Cardiovascular · 122d

Cardiovascular · 122d

Cleared Oct 27, 2016

CorPath GRX System

K160121 · DXX

Cardiovascular · 282d

Cleared Mar 18, 2016

CorPath 200 System

K152999 · DXX

Cardiovascular · 157d

Cleared Oct 02, 2015

CorPath 200 System

K150892 · DXX

Cardiovascular · 183d

Cleared Jul 19, 2012

CORPATH 200 SYSTEM

K120834 · DXX

Cardiovascular · 122d

Corindus, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Corindus, Inc.

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