Sterex Electrolysis Intl., Ltd.
United KingdomFDA applicant, unverified FDA FEI 1000439607
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Sterex Electrolysis Intl., Ltd. makes
Sterex Electrolysis Intl., Ltd. manufactures sterile, disposable electrolysis needles designed specifically for epilation procedures. These needles are intended for use in electrolysis machines to remove hair by destroying the hair follicle with electrical current.
The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000439607
- Address
- 174 KINGS RD.,, BIRMINGHAM
Frequently asked questions
How many devices does Sterex Electrolysis Intl., Ltd. have in the registry?
The registry currently lists 1 device for Sterex Electrolysis Intl., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sterex Electrolysis Intl., Ltd.'s devices?
Among its 1 most recently registered device, Sterex Electrolysis Intl., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Sterex Electrolysis Intl., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sterex Electrolysis Intl., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sterex Electrolysis Intl., Ltd. in the registry?
The most recently registered devices listed for Sterex Electrolysis Intl., Ltd. include STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION.