Winfield Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Winfield Co., Inc. makes
Winfield Co., Inc. manufactures medical devices including sharps containers with various features, latex examination gloves, and convalescent recliners.
The company's products are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Winfield Co., Inc. is based in the US.
Catalogue
Sharps-Tainer Large Opening Ref K942901
Regimes: 510(k) Registry: 510(k)Sharps-Tainer Small Opening W/Needle Remover Ref K942902
Regimes: 510(k) Registry: 510(k)Winfield Latex Examination Gloves Ref K891855
Regimes: 510(k) Registry: 510(k)Sharps-Tainer Small Opening Ref K942903
Regimes: 510(k) Registry: 510(k)Convalescent Recliner Ref K802803
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Winfield Co., Inc. have in the registry?
The registry currently lists 5 devices for Winfield Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Winfield Co., Inc.'s devices?
Among its 5 most recently registered devices, Winfield Co., Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Winfield Co., Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Winfield Co., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Winfield Co., Inc. in the registry?
The most recently registered devices listed for Winfield Co., Inc. include SHARPS-TAINER LARGE OPENING, SHARPS-TAINER SMALL OPENING W/NEEDLE REMOVER, WINFIELD LATEX EXAMINATION GLOVES and SHARPS-TAINER SMALL OPENING.