Medical Device Manufacturer · US , Farmington , CT

Avitus Orthopaedics, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2015

Total

Cleared

Denied

Avitus Orthopaedics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Farmington, US.

Last cleared in 2023. Active since 2015. Primary specialty: Gastroenterology & Urology.

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

510(k) submissions have been managed by Keystone Regulatory Services, LLC as regulatory consultant.

Avitus Orthopaedics, 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 - Avitus Orthopaedics, Inc.

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,450 total devices indexed.

Last updated: May 15, 2026