Singfar Ent. Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Singfar Ent. Co., Ltd. makes
Singfar Ent. Co., Ltd. manufactures patient examination gloves made of vinyl, intended for single‑use protective barrier applications in clinical settings.
These gloves are classified as Class I medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Patient Examination Gloves (Vinyl) Ref K892180
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Singfar Ent. Co., Ltd. have in the registry?
The registry currently lists 1 device for Singfar Ent. Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Singfar Ent. Co., Ltd.'s devices?
Among its 1 most recently registered device, Singfar Ent. Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Singfar Ent. Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Singfar Ent. Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Singfar Ent. Co., Ltd. in the registry?
The most recently registered devices listed for Singfar Ent. Co., Ltd. include PATIENT EXAMINATION GLOVES (VINYL).