Felton International, Inc. is one of 25357 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Felton International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HUMAN SUBCUTANEOUS INJECTOR, MODEL HSI 500, BI-3M NEEDLE-FREE INJECTOR SYSTEM
2
Total
2
Cleared
0
Denied
Felton International, Inc. has 2 FDA 510(k) cleared medical devices. Based in Lenexa, US.
Historical record: 2 cleared submissions from 2001 to 2004. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Felton International, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Felton International, Inc.
2 devices