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Cresilon, Inc.

FDA Regulatory Profile

Cresilon, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on December 12, 2025.

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K253609TRAUMAGEL® 2.0 Hemostatic GelDecember 12, 2025
K240713TRAUMAGEL®August 14, 2024
K213652Cresilon Hemostatic Gel, CHG, Cresilon Hemostatic Gel (CHG)June 28, 2023

FDA data resources