Haolang Medical USA Corporation
United Statesfrom the FDA registration address FDA establishment FEI 3016727301
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Haolang Medical USA Corporation makes
Haolang Medical USA Corporation manufactures vascular catheters, including umbilical vessel catheters, arterial catheters, and hemodialysis catheters designed for medical procedures requiring vascular access.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Umbilical Vessels Catheter Ref K201697
Regimes: 510(k) Registry: 510(k)Arterial Catheter Ref K201726
Regimes: 510(k) Registry: 510(k)Hemodialysis Catheter Ref K241581
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3016727301
- Address
- 8623 NE 26th Pl, Clyde Hill, WA, 98004
Frequently asked questions
How many devices does HAOLANG MEDICAL USA CORPORATION have in the registry?
The registry currently lists 3 devices for HAOLANG MEDICAL USA CORPORATION. Devices recorded under merged duplicate company entries are counted once.
Which registries list HAOLANG MEDICAL USA CORPORATION's devices?
Among its 3 most recently registered devices, HAOLANG MEDICAL USA CORPORATION has devices listed in FDA 510(k) (3 devices).
What risk classes do HAOLANG MEDICAL USA CORPORATION's devices fall under?
Among its 3 most recently registered devices, the classes recorded for HAOLANG MEDICAL USA CORPORATION's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from HAOLANG MEDICAL USA CORPORATION in the registry?
The most recently registered devices listed for HAOLANG MEDICAL USA CORPORATION include Umbilical Vessels Catheter, Arterial Catheter and Hemodialysis Catheter.