Anchor Innovation Medical (A.I.M.) is one of 18522 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Anchor Innovation Medical (A.I.M.) has 2 FDA 510(k) cleared medical devices. Based in Rockville, US.
Historical record: 2 cleared submissions from 2014 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Anchor Innovation Medical (A.I.M.) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Anchor Innovation Medical (A.I.M.)
2 devices