Manufacturer and brand owner in Wuqing District, Tianjin, China. 2 device types, 3 products catalogued, 1 clearance.
Tianjin Mastervision Technology Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Lens, Contact (Other Material) – Daily, Lens, Contact, Orthokeratology, Overnight. 3 of its products are catalogued under its own name. Its earliest product listing with the FDA dates from 2025.
Registration
FDA registration record for Tianjin Mastervision Technology Co., Ltd. | Registered name | TIANJIN MASTERVISION TECHNOLOGY CO., LTD. |
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3032010300 |
| FEI number | 3032010300 |
| DUNS | 729799269 |
| Establishment type | Manufacturer |
Chinese Registration
Chinese company register details for Tianjin Mastervision Technology Co., Ltd. | Chinese legal name | 天津视达佳科技有限公司 |
| Unified social credit code | 91120222094238078A |
| Source | NMPA UDI database |
Location
Address of Tianjin Mastervision Technology Co., Ltd. | City | Wuqing District |
| Province | Tianjin |
| Address | 1st Floor No.15 Building. No. 89 Heyuan Road |
| Postal code | 301700 |
| Country | China |
From the Company
Published by the company on its own website, not by the FDA.
Information published by Tianjin Mastervision Technology Co., Ltd. | Founded | 2014 |
| Main products | Rigid gas-permeable contact lenses |
PMA Approvals
A premarket approval is the Class III route: granted on clinical evidence, not on equivalence to a device already on the market.
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.