Unicable
Country not established
- Devices
- 1
What Unicable makes
Unicable manufactures latex patient examination gloves designed for clinical use, intended to provide barrier protection during medical examinations and procedures.
The company’s portfolio is regulated under FDA’s Class I device classification, with relevant products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Uni-Lab Patient Examination Gloves (Latex) Ref K892486
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Unicable have in the registry?
The registry currently lists 1 device for Unicable. Devices recorded under merged duplicate company entries are counted once.
Which registries list Unicable's devices?
Among its 1 most recently registered device, Unicable has devices listed in FDA 510(k) (1 device).
What risk classes do Unicable's devices fall under?
Among its 1 most recently registered device, the classes recorded for Unicable's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Unicable in the registry?
The most recently registered devices listed for Unicable include UNI-LAB PATIENT EXAMINATION GLOVES (LATEX).