FDA applicant
M.I.Tech Co., Ltd.
FDA records 14 decisions for M.I.Tech Co., Ltd. (Pyeongtaek-Si, KR) from 2008 to 2025: 14 510(k) clearances. Most are in product codes ESW (Prosthesis, Esophageal) and FGE (Stents, Drains And Dilators For The Biliary…). Since 2016 its 510(k)s took a median of 84 days from receipt to decision, against 139 for FDA’s reviews in the same codes and years. Its devices cite 16 predicates, 7 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided M.I.Tech Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2008.
Planning a device like M.I.Tech Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report