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Biolitec Medical Devices, Inc.

9 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
EVOLVE HPD 980/ 1470NM MULTIWAVELENGTH DIODE LASER (EVOLVE DUAL) (K120231)Biolitec Medical Devices, Inc.2012-04-24
MEGABEAM REUSABLE FIBER OPTIC DELIVERY SYSTEM (K113688)Biolitec Medical Devices, Inc.2012-03-13
MEGABEAM ENDO-ENT PROBE (K113858)Biolitec Medical Devices, Inc.2012-01-24
MEGABEAM FIBER OPTIC DELIVERY SYSTEM WITH ADDITIONAL TIPS & HANDPIECE (K113709)Biolitec Medical Devices, Inc.2012-01-20
MEGABEAM ENDOCULAR PROBE AND ASPIRATING ENDOCULAR PROBE (K113792)Biolitec Medical Devices, Inc.2012-01-19
TWISTER SIDE FIRE OPTICAL FIBER DELIVERY SYSTEM (K112987)Biolitec Medical Devices, Inc.2011-12-16
ENDOVASCULAR LASER VEIN SYSTEM KIT (K112299)Biolitec Medical Devices, Inc.2011-11-03
RADIAL-EMITTING SHAPED FIBER OPTIC DELIVERY SYSTEM (K112442)Biolitec Medical Devices, Inc.2011-09-30
CERALAS 980NM DIODE LASER FAMILY (K112324)Biolitec Medical Devices, Inc.2011-09-06

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Every clearance here is in the API, with alerts when new ones post.