Industri Leva Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Industri Leva Sdn. Bhd. makes
Industri Leva Sdn. Bhd. manufactures latex patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce contamination risk during clinical examinations.
The company’s product portfolio is classified under Class I medical devices and is listed in the FDA 510(k) registry under U.S. regulatory requirements. The manufacturer is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892749
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Industri Leva Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Industri Leva Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Industri Leva Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Industri Leva Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Industri Leva Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Industri Leva Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Industri Leva Sdn. Bhd. in the registry?
The most recently registered devices listed for Industri Leva Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX).