International Medical Devices Database

Manufacturer Parent Company (2017)
Stichting Administratiekantoor Opm
Source
NZMMDSA
1 Event
- Recall of Oculentis LENTIS HydroSmart foldable intraocular lens

One device in the database

Oculentis LENTIS HydroSmart foldable intraocular lens

Model / Serial
Model: All IOL models starting with L-, LU-, or LS-, Affected: Serial numbers starting with 20000

9 manufacturers with a similar name

Learn more about the data here

Oculentis GmbH

Manufacturer Parent Company (2017)
Stichting Administratiekantoor Opm
Source
LAANSM

Oculentis GmbH

Manufacturer Parent Company (2017)
Stichting Administratiekantoor Opm
Source
AEMPSVFOI

Oculentis GmbH

Manufacturer Parent Company (2017)
Stichting Administratiekantoor Opm
Source
BAM

Oculentis GmbH

Manufacturer Parent Company (2017)
Stichting Administratiekantoor Opm
Source
SMPA

Oculentis GmbH

Manufacturer Parent Company (2017)
Stichting Administratiekantoor Opm
Source
SATP

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Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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