Clareblend, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LUMAPROBE, CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Clareblend, Inc. General & Plastic Surgery ✕
3 devices