Tech Dyne Group
Country not established
- Devices
- 1
What Tech Dyne Group makes
Tech Dyne Group manufactures diagnostic and monitoring devices, including the HP-2000 (a handheld pressure measurement tool), SKREEN TEST (a screening device for specific physiological parameters), and the RMS-200 (a real-time monitoring system for signal analysis). These products are designed for clinical and point-of-care use to assess patient data in real time.
The company’s portfolio is regulated under FDA 510(k) clearance as Class II devices. These products are listed in the FDA’s 510(k) database, reflecting their compliance with U.S. medical device regulations. Tech Dyne Group operates from the United States.
Catalogue
Tech Dyne - Hp-2000, Skreen Test, Rms-200 Ref K920183
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tech Dyne Group have in the registry?
The registry currently lists 1 device for Tech Dyne Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tech Dyne Group's devices?
Among its 1 most recently registered device, Tech Dyne Group has devices listed in FDA 510(k) (1 device).
What risk classes do Tech Dyne Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Tech Dyne Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tech Dyne Group in the registry?
The most recently registered devices listed for Tech Dyne Group include TECH DYNE - HP-2000, SKREEN TEST, RMS-200.