Rodenstock GmbH
Munich-based premium spectacle lens and progressive lens manufacturer with biometrics-based lens…
Munich-based premium spectacle lens and progressive lens manufacturer with biometrics-based lens systems, present in over 85 countries with key markets in Germany, the US and China.
- Type
- Manufacturer
- Location
- Munich, Germany
- Founded
- 1877
- Website
- rodenstock.com
- Categories
- Eyewear & Sunglasses, Medical & Healthcare Supplies
- Markets
- Germany, United States, China, France, Australia
Verified facts
- registered-manufacturer (green), checked 2026-08-21 ALIMS (Medicines and Medical Devices Agency of Serbia), register of medical-device manufacturers
- domain-registered (green), checked 2026-08-02 Domain registry record
- vat-valid (green), checked 2026-08-22 VIES (European Commission)
- lei-active (green), checked 2026-08-23 GLEIF global LEI register (golden copy)
- sanctions-clear (green), checked 2026-08-16 OpenSanctions
- debarment-clear (green), checked 2026-08-16 OpenSanctions
- operating-permit (green), checked 2026-08-08 EEA Industrial Emissions Portal (IED), EU-wide permit register
- facility-registered (green), checked 2026-08-16 European Industrial Emissions Portal (E-PRTR / IED), European Environment Agency
- aeo-certified (green), checked 2026-08-16 EU AEO register (European Commission)
Profiles
Claimed certifications
- ISO 9001, Quality Management IAF CertSearch
- ISO 13485, Medical Devices Quality IAF CertSearch
- ISO 14001, Environmental Management IAF CertSearch
- 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)
- Sunglasses and protective eyewear are personal protective equipment in the EU: CE marking under Regulation (EU) 2016/425 is required. European Commission (PPE)