Crescom Co., Ltd.
South KoreaFDA 510(k) applicant, unverified
- Devices
- 2
What Crescom Co., Ltd. makes
Crescom Co., Ltd. manufactures the MediAI-BA, which is a medical device used for bone age assessment.
The company is based in the US, and its portfolio includes Class II devices that are listed in the FDA 510(k) registry.
Catalogue
Frequently asked questions
How many devices does Crescom Co., Ltd. have in the registry?
The registry currently lists 2 devices for Crescom Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Crescom Co., Ltd.'s devices?
Among its 2 most recently registered devices, Crescom Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Crescom Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Crescom Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Crescom Co., Ltd. in the registry?
The most recently registered devices listed for Crescom Co., Ltd. include MediAI-OA and MediAI-BA.