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EvoEndo, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251708EvoEndo Single-Use Endoscopy SystemOctober 10, 2025
K250900EvoEndo Single-Use Endoscopy SystemJune 16, 2025
K213606EvoEndo Single-Use Endoscopy SystemFebruary 14, 2022