Sterex Electrolysis Intl., Ltd. FDA Record
- No warning letters matched by name
Sterex Electrolysis Intl., Ltd. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Sterex Electrolysis Intl., Ltd." is on file.
- Latest 510(k)
- Oct 18, 1995
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 11, 2026 (checked Nov 15, 2026, unchanged) | File dated Nov 10, 2026 | Current |
| 510(k) clearances | 1 | Nov 15, 2026 | File dated Nov 9, 2026 | Current |
| Inspections | 0 | Nov 15, 2026 | Newest record Nov 5, 2026 | Current |
| Compliance actions | 0 | Nov 2, 2026 | Newest record Oct 29, 2026 | Current |
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Recent 510(k) clearances
| K-Number | Device | Date |
|---|---|---|
| K952611 | STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATION | Oct 18, 1995 |
Sterex Electrolysis Intl., Ltd. and the FDA: common questions
Has Sterex Electrolysis Intl., Ltd. received an FDA warning letter?
No FDA warning letter addressed to the name "Sterex Electrolysis Intl., Ltd." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.
Has Sterex Electrolysis Intl., Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Sterex Electrolysis Intl., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
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