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Eximo Medical, Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241553Auryon Atherectomy Catheter 1.7mm; Auryon Atherectomy Catheter 1.7mm, Hydrophilic CoatingJune 27, 2024
K233668Auryon Atherectomy Catheter 1.5 mm XL, Hydrophilic Coating (EXM-4010-H000), Auryon Atherectomy CatheDecember 15, 2023
K230709Auryon Atherectomy SystemJune 9, 2023
K220116Auryon Atherectomy CathetersSeptember 26, 2022
K221077Auryon Atherectomy SystemJune 9, 2022
K202835Auryon Atherectomy SystemDecember 2, 2020
K181642B-Laser Atherectomy SystemOctober 5, 2018