Shenzhen Goodwind Technology Development Co., Ltd. FDA Record
Shenzhen Goodwind Technology Development Co., Ltd. has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Shenzhen Goodwind Technology Development Co., Ltd." is on file.
- Latest 510(k)
- Aug 10, 2026
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 3 | 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 |
|---|---|---|
| K261602 | Eye Recovery Pro (PH-e03) | Aug 10, 2026 |
| K252983 | Wrinkle Retreat Pro Light Therapy Face Mask (Model: PH-m03) | Dec 17, 2025 |
| K222316 | IPL Hair Removal Device | Sep 28, 2022 |
Shenzhen Goodwind Technology Development Co., Ltd. and the FDA: common questions
Has Shenzhen Goodwind Technology Development Co., Ltd. received an FDA warning letter?
No FDA warning letter addressed to the name "Shenzhen Goodwind Technology Development Co., 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 Shenzhen Goodwind Technology Development Co., Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Shenzhen Goodwind Technology Development Co., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
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