ANTONMOVE is committed to global compliance and medical-grade safety standards. Our products are distributed under strict corporate governance and manufactured in partnership with certified medical device facilities.
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Corporate Entity
Hong Kong Business Registration
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Supply Chain Compliance
Class III Medical Device Sales License
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ISO 13485 Certified
Medical Devices Quality Management
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CE Certified
European Health & Safety Standards
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FDA Registered
US Medical Device Listing & Establishment
US CompliantSupply Chain & Compliance Transparency: ANTONMOVE brand operations are managed by our registered entity in Hong Kong, with domestic supply chain management supported by our Class III Medical Device licensed operation in China. All medical consumables (including sterile needles, cannula, and PDO threads) are manufactured in strict compliance with ISO 13485, CE, and FDA standards by our contract manufacturing partners.