Southland Products Co., Ltd.
ThailandFDA applicant, unverified
- Devices
- 3
What Southland Products Co., Ltd. makes
Southland Products Co., Ltd. manufactures powder-free, polymer-coated latex examination gloves, including variants with a protein label claim. These gloves are designed for patient examinations and medical procedures, providing a barrier against contamination while minimizing irritation risks.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are registered in the U.S. and comply with applicable U.S. regulatory requirements.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Patient Examination Gloves Ref K901903
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Southland Products Co., Ltd. have in the registry?
The registry currently lists 3 devices for Southland Products Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Southland Products Co., Ltd.'s devices?
Among its 3 most recently registered devices, Southland Products Co., Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Southland Products Co., Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Southland Products Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Southland Products Co., Ltd. in the registry?
The most recently registered devices listed for Southland Products Co., Ltd. include SOUTHLAND POWDERFREE (POLYMER-COATED) LATEX EXAMINATION GLOVES, PATIENT EXAMINATION GLOVES and SOUTHLAND POWDERFREE LATEX EXAMINATION GLOVES WITH PROTEIN LABEL CLAIM.