FDA applicant
Emg Technology Co., Ltd.
FDA records 11 decisions for Emg Technology Co., Ltd. (Hsin-Chu City, TW) from 2003 to 2011: 11 510(k) clearances. Most are in product codes JCX (Apparatus, Suction, Ward Use, Portable…) and ITI (Wheelchair, Powered). Its devices cite 7 predicates, 1 of them its own earlier devices. 3 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Emg Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2011
2026 so far, outlined.
Recalls per year
1in 2014
Class I Class II/III not classified
Planning a device like Emg Technology Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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