Jinnwah Ent., Inc.
Country not established
- Devices
- 1
What Jinnwah Ent., Inc. makes
Jinnwah Ent., Inc. manufactures latex patient examination gloves, designed for clinical use during medical 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
Patient Examination Gloves (Latex) Ref K892268
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jinnwah Ent., Inc. have in the registry?
The registry currently lists 1 device for Jinnwah Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jinnwah Ent., Inc.'s devices?
Among its 1 most recently registered device, Jinnwah Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Jinnwah Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jinnwah Ent., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jinnwah Ent., Inc. in the registry?
The most recently registered devices listed for Jinnwah Ent., Inc. include PATIENT EXAMINATION GLOVES (LATEX).