Anchor Innovation Medical (A.I.M.) - FDA 510(k) Cleared Devices
Recent clearances: A.I.M. Lead Loop Suturing Device (1), A.I.M. Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (1) plus Tension Assist/Suture Cutter Device, A.I.M. Lead Loop Suturing Device (2), A.I.M. Lead Loop Suturing Device plus Tension Assist/Suture Cutter Device, A.I.M. KNOTLESS MENISCAL REPAIR DEVICE
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Anchor Innovation Medical (A.I.M.) General & Plastic Surgery ✕
2 devices