Hightech Development
CzechiaFDA applicant, unverified
- Devices
- 1
What Hightech Development makes
Hightech Development manufactures electro-antiperspirant devices, including variants for standard use, sensitive skin, and premium performance (ELITE). These products use electrical stimulation to reduce underarm perspiration, targeting individuals seeking non-chemical sweat control solutions.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) clearance registry. The manufacturer operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hightech Development have in the registry?
The registry currently lists 1 device for Hightech Development. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hightech Development's devices?
Among its 1 most recently registered device, Hightech Development has devices listed in FDA 510(k) (1 device).
What risk classes do Hightech Development's devices fall under?
Among its 1 most recently registered device, the classes recorded for Hightech Development's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hightech Development in the registry?
The most recently registered devices listed for Hightech Development include Electro Antiperspirant, Electro Antiperspirant Sensitive, Electro Antiperspirant ELITE.