Gromax Rubber Industry Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
What Gromax Rubber Industry Co., Ltd. makes
Gromax Rubber Industry Co., Ltd. manufactures latex examination gloves, designed for medical and clinical use to provide barrier protection during patient examinations and procedures.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Latex Examination Gloves Ref K893302
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gromax Rubber Industry Co., Ltd. have in the registry?
The registry currently lists 1 device for Gromax Rubber Industry Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gromax Rubber Industry Co., Ltd.'s devices?
Among its 1 most recently registered device, Gromax Rubber Industry Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Gromax Rubber Industry Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gromax Rubber Industry Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gromax Rubber Industry Co., Ltd. in the registry?
The most recently registered devices listed for Gromax Rubber Industry Co., Ltd. include LATEX EXAMINATION GLOVES.