International Medical Devices Database

Manufacturer Address
Lumenis, Inc., 3959 W 1820 S, Salt Lake City UT 84104-4951
Manufacturer Parent Company (2017)
Laguna Holdco Ltd
Source
USFDA
1 Event
- Recall of Device Recall Laser Surgical Fiber

One device in the database

Device Recall Laser Surgical Fiber

Model / Serial
Lot number 61280807.
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
MA
Product Description
Boston Scientific SlimLine 200 Micron Holmium Fiber Delivery Device, Catalog No. 840-840, Sterile, Made In Israel, Manufactured By LUMENIS, P.O.Box 240, Yokneam, ISRAEL.

One manufacturer with a similar name

Learn more about the data here

Lumenis, Inc.

Manufacturer Address
Lumenis, Inc., 3959 W 1820 S, Salt Lake City UT 84104
Manufacturer Parent Company (2017)
Laguna Holdco Ltd
Source
USFDA

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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