Medical Device Manufacturer · CA , Quebec

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

5 submissions · 5 cleared · Since 2017

Total

Cleared

Denied

Genepoc, Inc. has 5 FDA 510(k) cleared medical devices. Based in Quebec, CA.

Historical record: 5 cleared submissions from 2017 to 2019. Primary specialty: Microbiology.

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

1 device has linked clinical trial registered on ClinicalTrials.gov.

Genepoc, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5