Promex Technologies, LLC
Country not established
- Devices
- 1
What Promex Technologies, LLC makes
Promex Technologies, LLC manufactures a full-core biopsy system designed for tissue sampling in medical diagnostics, enabling precise extraction of cylindrical core samples from tissue for histopathological analysis.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance in the United States. The manufacturer is based in the US.
Catalogue
Full Core Biopsy System Ref K111765
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promex Technologies, LLC have in the registry?
The registry currently lists 1 device for Promex Technologies, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promex Technologies, LLC's devices?
Among its 1 most recently registered device, Promex Technologies, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Promex Technologies, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Promex Technologies, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promex Technologies, LLC in the registry?
The most recently registered devices listed for Promex Technologies, LLC include FULL CORE BIOPSY SYSTEM.