Oura Health Oy
핀란드의 스마트링 및 건강 웨어러블 제조업체.
Oura는 수면, 준비, 활동 및 건강 통찰력을 위한 웨어러블 장치인 Oura Ring을 설계하고 제조합니다. 2013년 오울루에서 설립된 이 회사는 전 세계 소비자, 웰니스 파트너 및 기업 프로그램에 스마트 링을 배포합니다.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Oulu, Finland
- Founded
- 2013
- Website
- ouraring.com
- Categories
- 웨어러블 및 개인용 기기, 의료 및 건강 관리 용품
- Markets
- 핀란드, 미국, 독일, 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
- domain-registered (green), checked 2026-08-02 Domain registry record
- standards-mark-certified (green), checked 2026-08-16 EAEU unified register of certificates and declarations
- registry-id-verified (green), checked 2026-09-18 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- registry-activity (green), checked 2026-09-18 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- registry-active-global (green), checked 2026-07-09 Finnish Patent and Registration Office (PRH)
- places-goods-on-market (green), checked 2026-09-07 Registre national des producteurs (ADEME/SYDEREP), France
- tax-filing-active (green), checked 2026-09-18 Finnish Tax Administration, public corporate tax data 2024 (Verohallinto)
- registered-address (green), checked 2026-08-14 Finnish Patent and Registration Office, Trade Register (PRH/YTJ open data)
- vat-valid (green), checked 2026-07-09 VIES
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)