Walter Lorenz Surgical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LORENZ ORTHODONTIC ANCHORAGE SYSTEM, LORENZ TITANIUM FRACTURE / RECONSTRUCTION DEVICES AND PRE-BENT PLATES, LORENZ STERNAL CLOSURE SYSTEM
56
Total
56
Cleared
0
Denied
FDA 510(k) Regulatory Record - Walter Lorenz Surgical, Inc. General & Plastic Surgery ✕
3 devices