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Alleva Medical Devices

FDA Regulatory Profile

Alleva Medical Devices 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 October 3, 2025.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K251646extriCARE® 1000 Negative Pressure Wound Therapy SystemOctober 3, 2025
K221223extriCARE® 3000 Negative Wound Pressure Therapy SystemFebruary 9, 2023

FDA data resources