FDA applicant
Tianjin Mastervision Technology Co., Ltd.
FDA records 2 decisions for Tianjin Mastervision Technology Co., Ltd. (Tianjin, CN) from 2024 to 2026: 1 510(k) clearance and 1 original PMA approval. Most are in product codes HQD (Lens, Contact (Other Material) - Daily) and NUU (Lens, Contact, Orthokeratology, Overnight). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Tianjin MasterVision Technology Co., Ltd.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Tianjin Mastervision Technology Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2024
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2024.
Planning a device like Tianjin Mastervision Technology Co.…’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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