Inpro Technology Device Factory
ChinaFDA applicant, unverified FDA FEI 3009512322
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Inpro Technology Device Factory makes
Inpro Technology Device Factory makes synthetic vinyl examination gloves that are powder-free. These gloves are available in different labels and colors, such as yellow.
The company's portfolio is regulated as Class I devices and is listed in the fda_510k registry. Inpro Technology Device Factory is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3009512322
- Address
- No.10-1, Xingan Road East, Linqu, WEIFANG Shandong
Frequently asked questions
How many devices does Inpro Technology Device Factory have in the registry?
The registry currently lists 2 devices for Inpro Technology Device Factory. Devices recorded under merged duplicate company entries are counted once.
Which registries list Inpro Technology Device Factory's devices?
Among its 2 most recently registered devices, Inpro Technology Device Factory has devices listed in FDA 510(k) (2 devices).
What risk classes do Inpro Technology Device Factory's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Inpro Technology Device Factory's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Inpro Technology Device Factory in the registry?
The most recently registered devices listed for Inpro Technology Device Factory include Synthetic Vinyl Examination Gloves, Powder-Free, Yellow and SYNTHETIC VINYL EXAMINATION GLOVES, POWDER FREE (AND MULTIPLE LABELS).