Withings SAS
프랑스의 연결된 건강 기기 및 스마트 체중계 제조업체.
Withings는 스마트 체중계, 하이브리드 시계, 혈압 모니터, 수면 센서 및 연결된 건강 장치를 제조합니다. 2008년 프랑스에서 설립된 이 회사는 전 세계적으로 가전제품, 약국, 웰니스 및 의료 채널을 공급하고 있습니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Issy-les-Moulineaux, France
- Founded
- 2008
- Website
- withings.com
- Categories
- 웨어러블 및 개인용 기기, 의료 및 건강 관리 용품
- Markets
- 프랑스, 독일, 미국, 영국
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- registry-activity (green), effective since 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- workforce-on-record (green), effective since 2026-07-01 INSEE SIRENE (Registre national des entreprises)
- registered-since (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- web-presence-since (green), checked 2026-08-21 Internet Archive (Wayback)
- facility-registered (green), effective since 2026-08-01 INSEE SIRENE (Registre national des entreprises)
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- directors-on-file (green), checked 2026-09-18 INSEE Sirene (annuaire-entreprises)
- corporate-mail-on-domain (green), checked 2026-08-26 Mail server of the company domain
- domain-registered (green), checked 2026-08-26 Domain registry record
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- places-goods-on-market (green), checked 2026-09-07 Registre national des producteurs (ADEME/SYDEREP), France
- financials-published (green), effective since 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)
- sanctions-clear (green), checked 2026-08-26 OpenSanctions
- debarment-clear (green), checked 2026-08-26 OpenSanctions
- listed-in-registry (amber), checked 2026-08-26 BRIS, EU business registers interconnection (e-justice.europa.eu)
- export-registered (green), checked 2026-08-26 EU EORI validation (European Commission)
- registry-id-verified (green), effective since 2026-06-04 Annuaire des Entreprises (INSEE / INPI)
Claimed certifications, not confirmed by us
- 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)