FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

Niti-S Esophageal Stent; Esophageal TTS Stent

K Number: K243619 · Decision Oct 30, 2025
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
58
Applicant Total
16
Review Days
342

Basic Information

Device Name
Niti-S Esophageal Stent; Esophageal TTS Stent
K Number
K243619
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3610
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Taewoong Medical Co., Ltd.
Date Received
November 22, 2024
Decision Date
October 30, 2025
Product Code
ESW
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ESW Prosthesis, Esophageal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ESW), ordered by most recent decision date.

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Other Clearances by Taewoong Medical Co., Ltd.

K Number Device Name
K260962 Sphincterotome
K252648 Niti-S SPAXUS Stent
K251123 Niti-S Biliary Stent; Niti-S Biliary Slim M Stent
K250663 Niti-S Duodenal Comfort Stent, Niti-S Colonic Comfort Stent
K223067 Niti-S Duodenal Stent; Niti-S Colonic Comfort Stent
K223626 Niti-S Biliary Speed D Stent
K223256 Optimos™ Cystotome
K221482 Esophageal TTS Stent
K221071 Niti-S Biliary Slim M Stent
K211706 Esophageal TTS Stent
Search all 16 clearances from Taewoong Medical Co., Ltd. →