Sportwelding GmbH is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Sportwelding GmbH - FDA 510(k) Cleared Devices
Recent clearances: Fiji Anchor
1
Total
1
Cleared
0
Denied
Sportwelding GmbH has 1 FDA 510(k) cleared medical devices. Based in Schlieren, CH.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sportwelding GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Sportwelding GmbH
1 devices