Wise Industries Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Wise Industries Sdn. Bhd. makes
Wise Industries Sdn. Bhd. manufactures latex patient examination gloves designed for clinical use, intended to provide a barrier between healthcare providers and patients during medical examinations.
The company’s product portfolio is regulated under FDA’s Class I device classification and is listed in the FDA’s 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
Wise & Safe Patient Examination Gloves (Latex) Ref K891659
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wise Industries Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Wise Industries Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wise Industries Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Wise Industries Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Wise Industries Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Wise Industries Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Wise Industries Sdn. Bhd. in the registry?
The most recently registered devices listed for Wise Industries Sdn. Bhd. include WISE & SAFE PATIENT EXAMINATION GLOVES (LATEX).