Fine Spring Ent. Co., Ltd.
Country not established
- Devices
- 1
What Fine Spring Ent. Co., Ltd. makes
Fine Spring Ent. Co., Ltd. manufactures latex patient examination gloves designed for medical use, intended to provide barrier protection during clinical examinations and procedures.
The company’s portfolio is regulated under FDA’s Class I device classification, with relevant products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Patient Examination Glove (Latex) Ref K892035
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fine Spring Ent. Co., Ltd. have in the registry?
The registry currently lists 1 device for Fine Spring Ent. Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fine Spring Ent. Co., Ltd.'s devices?
Among its 1 most recently registered device, Fine Spring Ent. Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Fine Spring Ent. Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fine Spring Ent. Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Fine Spring Ent. Co., Ltd. in the registry?
The most recently registered devices listed for Fine Spring Ent. Co., Ltd. include PATIENT EXAMINATION GLOVE (LATEX).