Ossur hf.
आइसलैंडिक प्रोस्थेटिक्स, ब्रेसिंग और मोबिलिटी-डिवाइस निर्माता।
ओसूर कृत्रिम अंग, ऑस्टियोआर्थराइटिस ब्रेसिज़, चोट समर्थन और गतिशीलता उत्पादों का विकास और निर्माण करता है। 1971 में आइसलैंड में स्थापित, कंपनी दुनिया भर में क्लीनिकों, वितरकों और सहायक कंपनियों के माध्यम से चिकित्सा और खेल-गतिशीलता उपकरण बेचती है।
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Reykjavik, Iceland
- Founded
- 1971
- Website
- ossur.com
- Categories
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ, खेल का सामान और आउटडोर
- Markets
- आइसलैंड, संयुक्त राज्य, जर्मनी, यूनाइटेड किंगडम
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
- debarment-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- sanctions-clear (green), checked 2026-08-09 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- domain-registered (green), checked 2026-08-09 Domain registry record
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)