Celon AG Medical Instruments is one of 503 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Celon AG Medical Instruments - FDA 510(k) Cleared Devices
Recent clearances: OLYMPUS ESG-100, MODEL WB991046, CELON ENT SYSTEM
2
Total
2
Cleared
0
Denied
Celon AG Medical Instruments has 2 FDA 510(k) cleared medical devices. Based in Teltow, DE.
Historical record: 2 cleared submissions from 2003 to 2008. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Celon AG Medical Instruments Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Celon AG Medical Instruments
2 devices