Qualiman Industrial Co., Ltd. FDA Record
Qualiman Industrial Co., Ltd. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Qualiman Industrial Co., Ltd." is on file.
- Latest 510(k)
- Dec 18, 2009
Summary
| Records | Count | Last refreshed | Source as of | Status |
|---|---|---|---|---|
| Recalls | 0 | Nov 8, 2026 | File dated Nov 3, 2026 | Current |
| 510(k) clearances | 1 | 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 |
|---|---|---|
| K092910 | FLUID-FILLED TEETHER | Dec 18, 2009 |
Qualiman Industrial Co., Ltd. and the FDA: common questions
Has Qualiman Industrial Co., Ltd. received an FDA warning letter?
No FDA warning letter addressed to the name "Qualiman Industrial 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 Qualiman Industrial Co., Ltd. received an FDA Form 483?
FDA has not published a Form 483 for "Qualiman Industrial Co., Ltd." in its reading room. FDA publishes some Form 483s, not all of them.
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