Ottobock
Prosthetics, orthotics, wheelchairs and mobility products.
Ottobock manufactures prosthetics, orthotics, wheelchairs and mobility products from its Duderstadt operations. The company supplies healthcare systems, laboratories, OEM partners or regulated export customers across its listed primary markets.
- Type
- Manufacturer
- Location
- Duderstadt, Germany
- Founded
- 1919
- Website
- ottobock.com
- Categories
- Medical & Healthcare Supplies
- Markets
- Germany, United States, Japan, Australia
Verified facts
- debarment-clear (green), checked 2026-08-03 OpenSanctions
- sanctions-clear (green), checked 2026-08-03 OpenSanctions
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- vat-valid (green), checked 2026-08-03 VIES
- domain-registered (green), checked 2026-08-03 Domain registry record
- fda-registered (green), checked 2026-08-03 FDA
- media-mention (green), checked 2026-08-02 boerse-global.de
- certificate-page-on-site (amber), checked 2026-08-11 Company's own certification page
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- aeo-certified (green), checked 2026-08-16 EU AEO register (European Commission)
- corporate-mail-on-domain (green), checked 2026-08-03 Mail server of the company domain
Profiles
Claimed certifications
- ISO 13485, Medical Devices Quality IAF CertSearch
- CE Marking EU NANDO (notified bodies)
- FDA Registered FDA Establishment Registration
- AEO, Authorised Economic Operator EU AEO database
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)