Bosungmeditech Co., Ltd.
South KoreaFDA 510(k) applicant, unverified FDA FEI 3009130324
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Bosungmeditech Co., Ltd. makes
Bosungmeditech Co., Ltd. manufactures lancets, specifically the SafeLan and SafeLan-Pro product lines. These devices include various models such as the SafeLan 26G and 30G, which are used for capillary blood sampling.
The company is based in the US, and its portfolio consists of Class II medical devices. These products are listed in the FDA 510(k) regulatory registry.
Catalogue
- 510(k) 510(k)
Company details
- FDA FEI number
- 3009130324
- Address
- 1031-8 Daean-ro, Heungeop-myeon, Wonju-si Gangwon
Frequently asked questions
How many devices does Bosungmeditech Co., Ltd. have in the registry?
The registry currently lists 1 device for Bosungmeditech Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bosungmeditech Co., Ltd.'s devices?
Among its 1 most recently registered device, Bosungmeditech Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Bosungmeditech Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bosungmeditech Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bosungmeditech Co., Ltd. in the registry?
The most recently registered devices listed for Bosungmeditech Co., Ltd. include SafeLan® (2 models/SafeLan 26G, SafeLan 30G), SafeLan®-Pro (1 model/SafeLan®-Pro).