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Sentinel Medical Technologies,

FDA Regulatory Profile

Sentinel Medical Technologies, appears in FDA public data with 0 recalls, 3 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 4, 2026.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K260756TraumaGuard Intra-Abdominal Pressure-Sensing System (000-0221)September 4, 2026
K240057TraumaGuard Intra-abdominal Pressure Sensing SystemApril 17, 2024
K210570TraumaGuard Intra-abdominal Pressure Sensing SystemOctober 29, 2021

FDA data resources