Felda Rubber Corp.
MalaysiaFDA applicant, unverified
- Devices
- 2
What Felda Rubber Corp. makes
Felda Rubber Corp. manufactures powder-free latex examination gloves and latex patient examination gloves, designed for medical and clinical use to ensure barrier protection during procedures.
These products are classified as Class I medical devices and are listed under the FDA’s 510(k) pathway. The company operates from Malaysia.
Catalogue
Powder Free Latex Examination Gloves Ref K993820
Regimes: 510(k) Registry: 510(k)Patient Examination Gloves (Latex) Ref K891446
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Felda Rubber Corp. have in the registry?
The registry currently lists 2 devices for Felda Rubber Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Felda Rubber Corp.'s devices?
Among its 2 most recently registered devices, Felda Rubber Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Felda Rubber Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Felda Rubber Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Felda Rubber Corp. in the registry?
The most recently registered devices listed for Felda Rubber Corp. include POWDER FREE LATEX EXAMINATION GLOVES and PATIENT EXAMINATION GLOVES (LATEX).