Ever Surplus (Usa), Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Ever Surplus (Usa), Inc. makes
Ever Surplus (USA), Inc. manufactures latex patient examination gloves, designed for single-use medical and clinical examinations.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891975
510(k) 510(k)Patient Examination Gloves (Latex) Ref K891976
510(k) 510(k)
Frequently asked questions
How many devices does Ever Surplus (Usa), Inc. have in the registry?
The registry currently lists 2 devices for Ever Surplus (Usa), Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ever Surplus (Usa), Inc.'s devices?
Among its 2 most recently registered devices, Ever Surplus (Usa), Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Ever Surplus (Usa), Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Ever Surplus (Usa), Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ever Surplus (Usa), Inc. in the registry?
The most recently registered devices listed for Ever Surplus (Usa), Inc. include PATIENT EXAMINATION GLOVES (LATEX).