International Medical Devices Database

Manufacturer Address
Revision Optics Inc, 25651 Atlantic Ocean Dr Ste A1, Lake Forest CA 92630-8835
Manufacturer Parent Company (2017)
ReVision Optics Inc.
Source
USFDA
1 Event
- Recall of Device Recall Raindrop Near Vision Inlay

One device in the database

Device Recall Raindrop Near Vision Inlay

Model / Serial
multiple lots since 08/01/2016
Product Classification
Ophthalmic Devices
Device Class
3
Implanted device?
Yes
Distribution
US: AL, AZ, CA, FL, GA, HI, IL, IN, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NY, OH, OK, PA, SD, TN, TX, UT, WA
Product Description
Raindrop Near Vision Inlay, Model# RD1-1

One manufacturer with a similar name

Learn more about the data here

Revision Optics Inc.

Manufacturer Parent Company (2017)
ReVision Optics Inc.
Source
RLMPH

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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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