Duplex International Trading Limited FDA Record
Duplex International Trading Limited has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Duplex International Trading Limited" is on file.
- Latest 510(k)
- Aug 4, 2026
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 2 | Nov 8, 2026 | File dated Nov 2, 2026 | Current |
| Inspections | 0 | Nov 14, 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 |
|---|---|---|
| K261496 | LED Light Therapy Masks (PE748, PE749, PE756) | Aug 4, 2026 |
| K214101 | Project E Beauty LED Light Therapy Mask (Model: PE730) | Mar 23, 2022 |
Duplex International Trading Limited and the FDA: common questions
Has Duplex International Trading Limited received an FDA warning letter?
No FDA warning letter addressed to the name "Duplex International Trading Limited" 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 Duplex International Trading Limited received an FDA Form 483?
FDA has not published a Form 483 for "Duplex International Trading Limited" in its reading room. FDA publishes some Form 483s, not all of them.
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