By NORA YANG | Updated: 2025-06-17
ISO 13485 is available while FDA is to be ready in October 2025 and CE next year. The schedule is getting behind than what we planned earlier for the new plant. Assembly machinery transfer and OEM/ODM production would be our primary work before receiving the CE papers and we will do what's needed step by step to grow.
Please find more by:
Web: www.endotra.com
LinkedIn: https://www.linkedin.com/company/hjmed
Youtube: https://www.youtube.com/@jvmedical
B2B site: https://world-medical.en.made-in-china.com
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