Starlit Ent. Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Starlit Ent. Co., Ltd. makes
Starlit Ent. Co., Ltd. manufactures non-sterile patient examination gloves, designed for single-use clinical examinations and procedures.
These products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Non-Sterile Patient Examination Gloves Ref K892303
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Starlit Ent. Co., Ltd. have in the registry?
The registry currently lists 1 device for Starlit Ent. Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Starlit Ent. Co., Ltd.'s devices?
Among its 1 most recently registered device, Starlit Ent. Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Starlit Ent. Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Starlit Ent. Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Starlit Ent. Co., Ltd. in the registry?
The most recently registered devices listed for Starlit Ent. Co., Ltd. include NON-STERILE PATIENT EXAMINATION GLOVES.