Weiss Ent., Inc.
Country not established
- Devices
- 1
What Weiss Ent., Inc. makes
Weiss Ent., Inc. manufactures latex patient examination gloves designed for clinical use, providing a barrier for medical professionals during examinations and procedures.
These gloves are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearance records in the U.S. registry. The company is based in the United States.
Catalogue
Patient Examination Glove (Latex) Ref K892033
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Weiss Ent., Inc. have in the registry?
The registry currently lists 1 device for Weiss Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Weiss Ent., Inc.'s devices?
Among its 1 most recently registered device, Weiss Ent., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Weiss Ent., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Weiss Ent., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Weiss Ent., Inc. in the registry?
The most recently registered devices listed for Weiss Ent., Inc. include PATIENT EXAMINATION GLOVE (LATEX).