Manufacturer and brand owner in Huizhou, Guangdong, China. 10 device types, 8 products catalogued.
Tianck Medical Co., Ltd. is a manufacturer holding a current FDA establishment registration. The registration covers Trocar, Needle, Catheter and 8 other device types. 8 of its products are catalogued under its own name. Its earliest product listing with the FDA dates from 2021.
Registration
FDA registration record for Tianck Medical Co., Ltd. | Registered name | TIANCK MEDICAL CO.,LTD |
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3016950436 |
| FEI number | 3016950436 |
| DUNS | 418642903 |
| Establishment type | Manufacturer |
Location
Address of Tianck Medical Co., Ltd. | City | Huizhou |
| Province | Guangdong |
| Address | Building No.7, Wandong Zhigu industry park, Jiangjun East Road, Huiyang District |
| Postal code | 516213 |
| Country | China |
From the Company
Published by the company on its own website, not by the FDA.
Information published by Tianck Medical Co., Ltd. | Main products | Central venous catheters, Hemodialysis catheters, Invasive pressure sensors, Interventional devices, Urological devices |
| Export markets | Europe, Americas, multiple countries globally |
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.