Apex Technologies, Inc.
Country not established
- Devices
- 1
What Apex Technologies, Inc. makes
Apex Technologies, Inc. manufactures the Seminal Fluid Collection Kit™, a device designed for the collection and handling of seminal fluid samples in clinical or diagnostic settings.
The company’s product portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Seminal Fluid Collection Kit(Tm) Ref K864473
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Apex Technologies, Inc. have in the registry?
The registry currently lists 1 device for Apex Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Apex Technologies, Inc.'s devices?
Among its 1 most recently registered device, Apex Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Apex Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Apex Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Apex Technologies, Inc. in the registry?
The most recently registered devices listed for Apex Technologies, Inc. include SEMINAL FLUID COLLECTION KIT(TM).