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Advanced Research Medical, LLC

FDA Regulatory Profile

Summary

Total Recalls
1
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1698-2024Class IIADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible Curette Loop Blade, Part March 14, 2023

Recent 510(k) Clearances

K-NumberDeviceDate
K203373Advanced Research Medical Trident SI Screw SystemJanuary 22, 2021
K173947Lumbar Interbody Fusion System (OLLIF)July 25, 2018