Wartner USA B.V. is one of 691 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Wartner USA B.V. - FDA 510(k) Cleared Devices
Recent clearances: WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022)
1
Total
1
Cleared
0
Denied
Wartner USA B.V. has 1 FDA 510(k) cleared medical devices. Based in Richmond Hill, Ontario, CA.
Historical record: 1 cleared submissions from 2003 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Wartner USA B.V. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wartner USA B.V.
1 devices