Medical Device Manufacturer · US , Orinda , CA

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

14 submissions · 14 cleared · Since 2007

Recent clearances: Primary Relief, Drug Relief v1, ANSiStim-PP

Total

Cleared

Denied

Dyansys, Inc. has 14 FDA 510(k) cleared neurology devices. Based in Orinda, US.

Last cleared in 2022. Active since 2007.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

2 devices have linked clinical trials registered on ClinicalTrials.gov.

Dyansys, 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 - Dyansys, Inc.

14 devices

1-14 of 14

Cleared CT Sep 13, 2022

Cleared CT May 12, 2022

THE PORTABLE ANSISCOPE

K071168 · DPS

Cardiovascular · 126d

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

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

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