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Philips Consumer Lifestyle

Country not established

Devices
2
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Philips Consumer Lifestyle makes

Philips Consumer Lifestyle manufactures self-adhesive electrodes for medical monitoring and pulse relief devices designed to alleviate discomfort from peripheral neuropathy.

These products fall under FDA Class II regulation and are listed via the 510(k) clearance process. The company is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Philips Self-Adhesive Electrodes Ref K151033

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • PulseRelief Ref K151035

    Active Regimes: 510(k) Registry: 510(k) Class:II

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 1 recall initiated by Philips Consumer Lifestyle, initiated on 2018-02-02. By recorded status: 1 terminated. The reasons filed fall into these groups: performance or accuracy. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

Recalls initiated per year

  • 2017 0
  • 2018 1
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 0
  • 2018

    • 2 Feb 2018 Z-0689-2018 Class II Terminated Device may provide inaccurate measurements. Distribution: Domestic (2463 units) and Foreign (42678 units) Submission number: K100488

Frequently asked questions

How many devices does Philips Consumer Lifestyle have in the registry?

The registry currently lists 2 devices for Philips Consumer Lifestyle. Devices recorded under merged duplicate company entries are counted once.

Which registries list Philips Consumer Lifestyle's devices?

Among its 2 most recently registered devices, Philips Consumer Lifestyle has devices listed in FDA 510(k) (2 devices).

What risk classes do Philips Consumer Lifestyle's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Philips Consumer Lifestyle's devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Philips Consumer Lifestyle?

FDA recall records list 1 recall initiated by Philips Consumer Lifestyle, the most recent initiated on 2 Feb 2018. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Philips Consumer Lifestyle in the registry?

The most recently registered devices listed for Philips Consumer Lifestyle include Philips Self-Adhesive Electrodes and PulseRelief.

Generated automatically from registry data and not verified by a human reviewer.