Devices

Device Recall Luxtec MLX 300 Watt Xenon Light Source

Model / Serial
Serial numbers: 031009 0416410 035709 023210 102109 053510 126709 039810 0310710 0411210 057910 034910 065010 044110 064310 117209 602319 062010 022010 113009 090408 043510 117409 093108 051709 086908 118509 032510 057810 083109 043810 082708 030910 061408 054710 061310 084009 106509 053009 060110 412110 021709 033409 051109 072309 073708 080808 083408 084208 084808 092808 100808 104008 021809 071908 022609 070208 093208 103609 105609 105809 110309 110609 110709 110809 110909 111009 111109 111309 083208 090808 120308 010909 022709 075108 101209 104509 105109 106409 107809 108009 036509 122008 075208 010509 036009 061909 085209 073308 040309 031209 102309 062409 036709 122808 040709 121908 093608 101108 123308 051609 040909 010909 036209 127209 061509 106809 121808 040809 033910 036409 040209 103109 103708 121009 040909 034410 033710 122009 073809 113009 041160 076408 117409 060309 116709 075609 115009 117609 116309 074209 022309 043610 042710 032210 118709 035110 and 023410 057410 030710 116109 032310 073309 and 1110109
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide, Canada, Australia, Germany, Netherlands, New Zealand, Norway, Singapore and Sweden
Product Description
Luxtec¿ MLX 300 Watt Xenon Light Source, || Model OOMLX; Surgical/Medical Light Source || This light source is designed to supply high-intensity light to a fiber optic cable for illumination of a surgical field during a surgical and/or medical procedure.
Manufacturer
Integra LifeSciences Corp.
1 Event
- Recall of Device Recall Luxtec MLX 300 Watt Xenon Light Source

Manufacturer

Integra LifeSciences Corp.

Manufacturer Address
Integra LifeSciences Corp., 311 Enterprise Dr, Plainsboro NJ 08536-3344
Manufacturer Parent Company (2017)
Integra LifeSciences Holdings Corporation
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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