Feilo Sylvania Germany GmbH FDA Record
- No warning letters matched by name
Feilo Sylvania Germany GmbH has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Feilo Sylvania Germany GmbH" 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 |
|---|---|---|
| K180581 | UV Lamps for Sunlamp Products | Jun 22, 2018 |
Feilo Sylvania Germany GmbH and the FDA: common questions
Has Feilo Sylvania Germany GmbH received an FDA warning letter?
No FDA warning letter addressed to the name "Feilo Sylvania Germany GmbH" 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 Feilo Sylvania Germany GmbH received an FDA Form 483?
FDA has not published a Form 483 for "Feilo Sylvania Germany GmbH" in its reading room. FDA publishes some Form 483s, not all of them.
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