Withings SAS
French connected health-device and smart-scale manufacturer.
Withings manufactures smart scales, hybrid watches, blood-pressure monitors, sleep sensors, and connected health devices. Founded in France in 2008, the company supplies consumer-electronics, pharmacy, wellness, and healthcare channels worldwide.
- Type
- Manufacturer
- Location
- Issy-les-Moulineaux, France
- Founded
- 2008
- Website
- withings.com
- Categories
- Wearables & Personal Devices, Medical & Healthcare Supplies
- Markets
- France, Germany, United States, United Kingdom
Verified facts
- workforce-on-record (green), checked 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- registered-manufacturer (green), checked 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- facility-registered (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- domain-registered (green), checked 2026-08-20 Domain registry record
- registered-since (green), checked 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- places-goods-on-market (green), checked 2026-08-16 Registre national des producteurs (ADEME/SYDEREP), France
- financials-published (green), checked 2023-12-31 INPI/BCE published accounts (data.economie.gouv.fr)
- registry-active-global (green), checked 2026-08-07 INSEE SIRENE (Registre national des entreprises)
- registry-id-verified (green), checked 2026-06-04 Annuaire des Entreprises (INSEE / INPI)
Claimed certifications
- EAC mark (EAEU conformity) EAEU unified register of certificates and declarations
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)
- Electronics for the EU need CE marking incl. RoHS substance limits, and producers must register for WEEE take-back in each member state of sale. European Commission (CE)
- Electronics for the US market need FCC equipment authorization under 47 CFR Part 15, which covers unintentional radiators such as switch-mode power supplies, not only radio devices. US FCC (Part 15)