Devices

Device Recall Endo Ocular Directional Laser Probe

Model / Serial
Model numbers: GA-0040061;, GA-0040062; GA-0040063; GA-0040064; GA-0040065 and GA-0040066 Lot numbers: 942439; 946478; 947498; 942440; 947496; 010120; and 947501
Product Classification
Ophthalmic Devices
Device Class
2
Implanted device?
No
Distribution
FL, IL, MD, CO and TX
Product Description
Endo Ocular Directional Laser Probe, Lumenis Inc. Salt Lake City, UT STERILE EO
Manufacturer
Lumenis, Inc.
1 Event
- Recall of Device Recall Endo Ocular Directional Laser Probe

Manufacturer

Lumenis, Inc.

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

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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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