Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in NetherlandsLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Royal Philips and its 1 subsidiaries with 11 510(k) clearances and 2 warning letters. The most recent is a warning letter dated Sep 9, 2025: Warning letter: Complaint handling, MDR reporting.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date, Royal Philips and its 1 subsidiaries
A hatched bar is a year that is not over, so its count covers only part of the year.
| Sep 9, 2025 | Warning letter: Complaint handling, MDR reportingCDRH | Warning letters |
| Feb 23, 2024 | Warning letter: Process validation, 510(k) requiredCDRH | Warning letters |
| Jan 24, 1992 | PHILIPS 41 SERIES RAINBOWK920134 · ESD | 510(k) clearances |
| Jan 23, 1992 | PHILIPS M60 SERIESK920142 · ESD | 510(k) clearances |
| Jun 27, 1985 | PHILIPS SOLARIUM HP 3134K852348 · FTC | 510(k) clearances |
| May 1, 1985 | PHILIPS UV-A SDARIUM TYPE HP 3148(CFR 21 SUNLAMPK851533 · FTC | 510(k) clearances |
| May 1, 1985 | PHILIPS UV-A SOLARIUM TYPE HP 3140K851535 · FTC | 510(k) clearances |
| May 1, 1985 | PHILIPS UV-A SOLARIUM TYPE HP 3150K851534 · FTC | 510(k) clearances |
| May 1, 1985 | PHILIPS UV-A SOLARIUM TYPE HP 3141K851536 · FTC | 510(k) clearances |
| Feb 21, 1985 | PHILIPS UV-A SOLARIUM TYPE HP 3126-SUNLAMPK850206 · FTC | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
