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Anchor Innovation Medical (A.I.M.)

FDA Regulatory Profile

Anchor Innovation Medical (A.I.M.) appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 27, 2015.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K150924A.I.M. Lead Loop Suturing Device (1), A.I.M. Tension Assist/Suture Cutter Device, A.I.M. Lead Loop SJuly 27, 2015
K133770A.I.M. KNOTLESS MENISCAL REPAIR DEVICEJune 10, 2014

FDA data resources