510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
MUMClass II

Stent, Metallic, Expandable, Duodenal

21 CFR 878.3610 / General, Plastic Surgery
FDA source (opens on fda.gov)

MUM is the FDA product code for Stent, Metallic, Expandable, Duodenal, a class II device type, regulated under 21 CFR 878.3610. As of , FDA records hold 6 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
MUM
Device name
Stent, Metallic, Expandable, Duodenal
Regulation
21 CFR 878.3610
Device class
Class II
Review panel
General, Plastic Surgery
Submission type
510(k)
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
6
Ingested recalls
0

Clearances, product code MUM

By decision year
6 clearances under product code MUM with a decision year between 1998 and 2025, 1998 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code MUM by decision year
YearClearances
19981
20061
20111
20171
20231
20251

Applicants with the most clearances

Product code MUM
Applicants holding the most 510(k) clearances under product code MUM
ApplicantClearances
Boston Scientific Corporation2
Cook Ireland Ltd.2
Taewoong Medical Co., Ltd.2

Companies listing this code with FDA

Companies whose registered establishments list this code