Medical Device Manufacturer · US , Sound Beach , NY

Stihler Electronic GmbH - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1999

Total

Cleared

Denied

Stihler Electronic GmbH has 6 FDA 510(k) cleared medical devices. Based in Sound Beach, US.

Historical record: 6 cleared submissions from 1999 to 2020.

Browse the FDA 510(k) cleared devices submitted by Stihler Electronic GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.

Stihler Electronic GmbH 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 - Stihler Electronic GmbH

6 devices

1-6 of 6