Haolang Technology (Foshan) Limited Corporation
Registered establishment in Foshan, Guangdong, China. 6 device types.
Haolang Technology (Foshan) Limited Corporation is a contract manufacturer holding a current FDA establishment registration. The registration covers Catheter, Percutaneous, Catheter, Umbilical Artery and 4 other device types. Its earliest product listing with the FDA dates from 2020.
Registration
| Registered name | HAOLANG TECHNOLOGY (FOSHAN) LIMITED CORPORATION |
|---|---|
| Status | Registered |
| Registration expires | 2026 |
| Registration number | 3006942602 |
| FEI number | 3006942602 |
| Establishment type | Contract manufacturer, Contract steriliser, Manufacturer |
Chinese Registration
| Chinese legal name | 昊朗科技（佛山）有限公司 |
|---|---|
| Unified social credit code | 914406007879332335 |
| Source | export sales certificate, Guangdong medical products administration |
Location
| City | Foshan |
|---|---|
| Province | Guangdong |
| Address | Xinyuan 2nd RD, Jili Industrial Park, Nanzhuang, ChanCheng District |
| Postal code | 528061 |
| Country | China |
What It Makes
| Device type | Class | Listed under the names | Listed since | Chinese makers |
|---|---|---|---|---|
| Catheter, Hemodialysis, Implanted | Class 2 | Hemodialysis Catheter | 2025 | 2 |
| Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days | Class 2 | Peripherally Inserted Central Catheter | 2020 | 5 |
| Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days | Class 2 | Midline Catheter, CT CVC | 2020 | 12 |
| Catheter, Percutaneous | Class 2 | Arterial Catheter | 2021 | 14 |
| Catheter, Umbilical Artery | Class 2 | Umbilical Vessels Catheter | 2021 | 1 |
| Set, Administration, Intravascular | Class 2 | Needle-Less Valve | 2020 | 49 |
From the Company
Published by the company on its own website, not by the FDA.
| Founded | 2006 |
|---|---|
| Employees | 300+ |
| Main products | central venous catheters, PICC, hemodialysis catheters, midline catheters |
| Certifications | FDA |
Nearby Manufacturers
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.
The manufacturer named here can complete this record.