Shijiazhuang Recovery Star Medical Device Co., Ltd. FDA Record
- No warning letters matched by name
Shijiazhuang Recovery Star Medical Device Co., Ltd. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Shijiazhuang Recovery Star Medical Device Co., Ltd." is on file.
- Latest 510(k)
- Oct 5, 2026
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 |
|---|---|---|
| K262285 | UV Phototherapy Device (KZX-308nm-BL65, KZX-308nm-BL55, KZX-308nm-BL50, KZX-308nm-BL45… | Oct 5, 2026 |
Shijiazhuang Recovery Star Medical Device Co., Ltd. and the FDA: common questions
Has Shijiazhuang Recovery Star Medical Device Co., Ltd. received an FDA warning letter?
No FDA warning letter addressed to the name "Shijiazhuang Recovery Star Medical Device 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 Shijiazhuang Recovery Star Medical Device Co., Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Shijiazhuang Recovery Star Medical Device Co., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
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