Meticuly Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: METICULY Patient-specific titanium mesh implant, METICULY Patient-specific titanium maxillofacial mesh implant, Meticuly Patient-Specific Titanium Mesh Implant
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Meticuly Co., Ltd. Neurology ✕
2 devices