Teh Loong Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Teh Loong Corp. makes
Teh Loong Corp. manufactures powdered and powder-free synthetic vinyl patient examination gloves in white and yellow. These gloves are designed for single-use medical and clinical examinations to provide barrier protection for both patients and healthcare providers.
The company’s products are classified as Class I medical devices under FDA regulations and are listed in the FDA’s 510(k) database. Teh Loong Corp. is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Teh Loong Corp. have in the registry?
The registry currently lists 3 devices for Teh Loong Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Teh Loong Corp.'s devices?
Among its 3 most recently registered devices, Teh Loong Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Teh Loong Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Teh Loong Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Teh Loong Corp. in the registry?
The most recently registered devices listed for Teh Loong Corp. include TEH LOONG POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, WHITE, TEH LOONG POWDER FREE SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW and TEH LOONG POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES, YELLOW.