International Medical Devices Database

Manufacturer Parent Company (2017)
HOYA Corp.
Source
RLMPH
1 Event
- Recall of Implants, non active, intraocular lens, Hoya-AF-1 iMICS1, AF-1 toric, iSERT and iSERT toric

One device in the database

Implants, non active, intraocular lens, Hoya-AF-1 iMICS1, AF-1 toric, iSERT and iSERT toric

Model / Serial

34 manufacturers with a similar name

Learn more about the data here

Hoya Corporation Pentax Miyagi Factory || Hoya Corporation

Manufacturer Parent Company (2017)
HOYA Corp.
Source
NIDFSINVIMA

Hoya Corporation Pentax Miyagi Factory || Pentax Medical Company

Manufacturer Parent Company (2017)
HOYA Corp.
Source
NIDFSINVIMA

HOYA CORPORATION

Manufacturer Parent Company (2017)
HOYA Corp.
Source
PMDAJ

HOYA CORPORATION

Manufacturer Parent Company (2017)
HOYA Corp.
Source
MSHM

HOYA Corporation

Manufacturer Parent Company (2017)
HOYA Corp.
Source
AEMPSVFOI

About this database

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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