Dura Corp., The FDA Record
Dura Corp., The has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Dura Corp., The" is on file.
- Latest 510(k)
- Jan 3, 1978
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 |
|---|---|---|
| K772322 | DEPILATORY, ELECTRONIC | Jan 3, 1978 |
Dura Corp., The and the FDA: common questions
Has Dura Corp., The received an FDA warning letter?
No FDA warning letter addressed to the name "Dura Corp., The" 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 Dura Corp., The received an FDA Form 483?
FDA has not published a Form 483 for "Dura Corp., The" in its reading room. FDA publishes some Form 483s, not all of them.
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