10 results
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65ms
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Sources: EU EUDAMED, US FDA
Lumitex Medical Devices, Inc.
Manufacturer
🇺🇸 United States
Lumitex Medical Devices, Inc.
Manufacturer
🇺🇸 United States·2 Importers
Lumitex Medical Devices, Inc.
FDA registration
Lumitex Medical Devices, Inc.·3 products·🇺🇸 United States
MLX 300W XENON LIGHTSOURCE
FDA Adverse Event
Malfunction
·INTEGRA BURLINGTON, MA, INC.·Product code FST·June 25, 2012
GIRAFFE SPOT PT(LED)
FDA Adverse Event
Injury
·LUMITEX MEDICAL DEVICES, INC.·Product code LBI·October 4, 2024
BILISOFT 2.0
FDA Adverse Event
Malfunction
·LUMITEX MEDICAL DEVICES, INC·Product code LBI·January 2, 2026
Ultra-Thin LightMat Surgical Illuminator, Disposable one time use. Model Number: UA2550, Exp Date: 2012-05. Product is packaged in individual sterile pouch w/5 pouches per box. The LightMat is intended for the illumination of surgical procedures, particularly where deep cavities or adjacent tissues limit outside light in the surgical field.
FDA Recall
Terminated
·Lumitex Inc·Product code FDG·July 1, 2009
MDSS GmbH
Authorized representative
🇩🇪 Germany·388 Manufacturers·16562 Devices
Stryker EMEA Supply Chain Services BV
Importer
🇳🇱 Netherlands·48 Manufacturers
Duomed Belgium NV
Importer
🇧🇪 Belgium·62 Manufacturers