Alizor, Inc. Dba Global Tech
Country not established
- Devices
- 1
What Alizor, Inc. Dba Global Tech makes
Alizor, Inc. dba Global Tech manufactures latex patient examination gloves.
These gloves are classified as Class I medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892032
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alizor, Inc. Dba Global Tech have in the registry?
The registry currently lists 1 device for Alizor, Inc. Dba Global Tech. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alizor, Inc. Dba Global Tech's devices?
Among its 1 most recently registered device, Alizor, Inc. Dba Global Tech has devices listed in FDA 510(k) (1 device).
What risk classes do Alizor, Inc. Dba Global Tech's devices fall under?
Among its 1 most recently registered device, the classes recorded for Alizor, Inc. Dba Global Tech's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Alizor, Inc. Dba Global Tech in the registry?
The most recently registered devices listed for Alizor, Inc. Dba Global Tech include PATIENT EXAMINATION GLOVES (LATEX).