Oura Health Oy
Finse fabrikant van slimme ringen en gezondheidswearables.
Oura ontwerpt en produceert de Oura Ring, een draagbaar apparaat voor inzicht in slaap, paraatheid, activiteit en gezondheid. Het bedrijf, opgericht in Oulu in 2013, distribueert slimme ringen aan consumenten, welzijnspartners en ondernemingsprogramma's wereldwijd.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Oulu, Finland
- Founded
- 2013
- Website
- ouraring.com
- Categories
- Wearables en persoonlijke apparaten, Medische en gezondheidszorgbenodigdheden
- Markets
- Finland, Verenigde Staten, Duitsland, Verenigd Koninkrijk
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)