Philips Consumer Lifestyle
Consumer health companyAI in NetherlandsAI, part of PhilipsAI. FDA records under 3 spellings of its name, each linked to the record.
- 510(k) clearances: 5
- Device recalls: 1
Records by Year
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
Latest Records
Newest first across sources; each opens the record| Date | Record | Source |
|---|---|---|
| Sep 3, 2026 | Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model: SCF593/52, SCF593/62); Philips Avent Natural Care Warming Hands-free Wearable Electric Breast Pump (Model: SCF594/52, SCF594/62)K261622 · HGX | 510(k) clearances |
| Dec 23, 2025 | Philips Lumea IPLK253754 · OHT | 510(k) clearances |
| Feb 10, 2025 | Philips Lumea IPLK243453 · OHT | 510(k) clearances |
| Feb 2, 2018 | Philips Avent Smart Ear Thermometer (SCH740), Philips Ear Thermometer (DL8740)Class II · Device may provide inaccurate measurements. | Device recalls |
| Jul 28, 2015 | Philips Self-Adhesive ElectrodesK151033 · GXY | 510(k) clearances |
| Jul 21, 2015 | PulseReliefK151035 · NUH | 510(k) clearances |
Canada and Imports
Matched by company name- Active Health Canada device licences
- 1, as of Nov 10, 2026
Names and Identifiers
- Appears as
- Website
- philips.com
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