Intl. Visco Group
Country not established
- Devices
- 1
What Intl. Visco Group makes
The company manufactures patient exam gloves, designed for single-use medical examinations and procedures. These gloves are produced using a proprietary polymer formulation to ensure durability and tactile sensitivity during clinical assessments.
The product portfolio is classified under FDA’s Class I regulatory category, with individual devices authorised via the 510(k) clearance pathway. The company’s devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Intl. Visco Group have in the registry?
The registry currently lists 1 device for Intl. Visco Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Intl. Visco Group's devices?
Among its 1 most recently registered device, Intl. Visco Group has devices listed in FDA 510(k) (1 device).
What risk classes do Intl. Visco Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Intl. Visco Group's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Intl. Visco Group in the registry?
The most recently registered devices listed for Intl. Visco Group include PATIENT EXAM GLOVES (MFG. POLYMINT INDUSTRIAL CO.).