Denver Splint Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Denver Splint Co. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Denver Splint Co. has 4 FDA 510(k) cleared medical devices. Based in Englewood, US.
Historical record: 4 cleared submissions from 1993 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Denver Splint Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Denver Splint Co.
4 devices