Kdb Inc. (Dba) Sperti Sunlamp FDA Record
- No warning letters matched by name
Kdb Inc. (Dba) Sperti Sunlamp has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Kdb Inc. (Dba) Sperti Sunlamp" is on file.
- Latest 510(k)
- Jun 22, 2018
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 |
|---|---|---|
| K151721 | FIJI SUN FLUORESCENT TANNING UNIT | Jun 22, 2018 |
Kdb Inc. (Dba) Sperti Sunlamp and the FDA: common questions
Has Kdb Inc. (Dba) Sperti Sunlamp received an FDA warning letter?
No FDA warning letter addressed to the name "Kdb Inc. (Dba) Sperti Sunlamp" 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 Kdb Inc. (Dba) Sperti Sunlamp received an FDA Form 483?
FDA has not published a Form 483 for "Kdb Inc. (Dba) Sperti Sunlamp" in its reading room. FDA publishes some Form 483s, not all of them.
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