Kleartex Sdn Bhd
Country not established
- Devices
- 2
What Kleartex Sdn Bhd makes
Kleartex Sdn Bhd manufactures latex surgeons' gloves and patient examination gloves, designed for single-use in clinical and medical examination settings.
These products are classified as Class I medical devices and are listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Kleartex Latex Surgeons Gloves Ref K904361
Regimes: 510(k) Registry: 510(k)Patient Examination Glove Ref K890975
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kleartex Sdn Bhd have in the registry?
The registry currently lists 2 devices for Kleartex Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kleartex Sdn Bhd's devices?
Among its 2 most recently registered devices, Kleartex Sdn Bhd has devices listed in FDA 510(k) (2 devices).
What risk classes do Kleartex Sdn Bhd's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kleartex Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kleartex Sdn Bhd in the registry?
The most recently registered devices listed for Kleartex Sdn Bhd include KLEARTEX LATEX SURGEONS GLOVES and PATIENT EXAMINATION GLOVE.