Cinderella Ent. Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Cinderella Ent. Co., Ltd. makes
Cinderella Ent. Co., Ltd. manufactures latex patient examination gloves designed for clinical use, ensuring barrier protection during medical procedures.
These gloves 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
Patient Examination Gloves (Latex) Ref K891493
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cinderella Ent. Co., Ltd. have in the registry?
The registry currently lists 1 device for Cinderella Ent. Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cinderella Ent. Co., Ltd.'s devices?
Among its 1 most recently registered device, Cinderella Ent. Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cinderella Ent. Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cinderella Ent. Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cinderella Ent. Co., Ltd. in the registry?
The most recently registered devices listed for Cinderella Ent. Co., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).