Kolster Methods is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kolster Methods - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Kolster Methods has 3 FDA 510(k) cleared medical devices. Based in Fullerton, US.
Historical record: 3 cleared submissions from 1989 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Kolster Methods Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kolster Methods
3 devices