M.I.Tech Co., Ltd.

M.I.Tech Co., Ltd. holds 14 FDA 510(k) medical device clearances, first cleared 2008, most recent 2025.

Top product codes for M.I.Tech Co., Ltd.

ESW — General, Plastic Surgery6 devices
FGE — Gastroenterology, Urology3 devices
MQR — General, Plastic Surgery3 devices
JCT — General, Plastic Surgery1 device
NUH — Neurology1 device

Recent clearances by M.I.Tech Co., Ltd.

K253327 — HANAROSTENT Esophagus Upper (CCC)Code ESW·2025-10-30
K213251 — HANAROSTENT Esophagus Asymmetric (CCC)Code ESW·2021-11-18
K201160 — HANAROSTENT Esophagus (CCC), HANAROSTENT Esophagus (NCN)Code ESW·2021-07-23
K202973 — HANAROSTENT Benefit Biliary (NNN)Code FGE·2021-05-11
K201342 — HANAROSTENT Trachea/Bronchium (CCC)Code JCT·2020-12-31
K200860 — HANAROSTENT Esophagus TTS (CCC), HANAROSTENT Esophagus TTS (NCN)Code ESW·2020-05-20
K190141 — HANAROSTENT LowAx Colon/Rectum (NNN)Code MQR·2019-03-07
K183396 — HANAROSTENT FASTTM Biliary (NNN)Code FGE·2019-02-11
K183616 — HANAROSTENT LowAx Colon/Rectum (NNN), HANAROSTENT LowAx Duodenum/Pylorus (NNN)Code MQR·2019-01-10
K180180 — HANAROSTENT LowAxTM Colon/Rectum (NNN), HANAROSTENT LowAxTM Duodenum/Pylorus (NNN)Code MQR·2018-11-02
K160893 — HANAROCare ReJuCode NUH·2016-07-27
K111149 — HANAROSTENT BILIARY (NNN)Code FGE·2011-12-30
K093537 — HANAROSTENT ESOPHAGUS (CCC)Code ESW·2010-06-04
K072094 — CHOOSTENTCode ESW·2008-09-25

Data sourced from openFDA. This site is unofficial and independent of the FDA.