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S&G Biotech, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K242845
EGIS Biliary Double Bare Stent (BDB080405)
June 25, 2025
K223354
EGIS Biliary Single Bare Stent
September 21, 2023