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MUM

Stent, Metallic, Expandable, Duodenal

Product code
MUM
Device name
Stent, Metallic, Expandable, Duodenal
Device class
Class 2
21 CFR
21 CFR 878.3610
Medical specialty
General, Plastic Surgery
Marketing pathway
510(K)
Flag
Implant
510(k) clearances (last 3 years)
1
Summaries archived here
1 (direct download)
510(k) clearances (all years, FDA)
6 (all years; only the last 3 years are listed here)

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2025-03-31.

NumberDecision dateApplicantDevice nameSummary
K2506632025-03-31Taewoong Medical Co., Ltd.Niti-S Duodenal Comfort Stent, Niti-S Colonic Comfor…PDF

1 summaries are archived here for direct download.

Official FDA classification page: MUM
Classification and pathway per current FDA publications. Data from openFDA (CC0).