Pimex Co., Ltd.
Country not established
- Devices
- 1
What Pimex Co., Ltd. makes
Pimex Co., Ltd. manufactures spectacle frames, which are non-invasive optical devices designed to support eyeglasses for vision correction.
The company’s spectacle frames are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The products are based in the United States.
Catalogue
Spectacle Frame Ref K943083
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pimex Co., Ltd. have in the registry?
The registry currently lists 1 device for Pimex Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pimex Co., Ltd.'s devices?
Among its 1 most recently registered device, Pimex Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Pimex Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pimex Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pimex Co., Ltd. in the registry?
The most recently registered devices listed for Pimex Co., Ltd. include SPECTACLE FRAME.