Data / Medical devices / United Kingdom / Sterex Electrolysis Intl., Ltd.
Sterex Electrolysis Intl., Ltd.: FDA-registered device maker in Birmingham, United Kingdom, 1 510(k) clearance
Sterex Electrolysis Intl., Ltd. is registered with the FDA (registration 9681366) in Birmingham, United Kingdom. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 18, 1995. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 9681366
- FEI number
- 1000439607
- Address
- 174 Kings RD., Tyseley, Birmingham, United Kingdom, B11 2AP
- Owner or operator
- STEREX ELECTROLYSIS INTL., LTD. (9022281)
- Roles
- Manufacturer
- First device listed
- November 30, 2007
- Registered through
- 2026
- Brand names listed
- sterex
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Epilator, High Frequency, Needle-Type | KCW | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 18, 1995 | K952611 | STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION | KCW | Substantially Equivalent | Sterex Electrolysis Intl., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 18, 1995. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.