Biolitec, Inc.
FDA 510(k) medical device clearances.
Top product codes for Biolitec, Inc.
Recent clearances by Biolitec, Inc.
- K112013 — EVOLVE(R) HPD 980/1470NM MULTIWAVELENGTH DIODE LASER
- K112253 — CERALAS 147NM DIODE LASER SYSTEM
- K110080 — RADIAL-EMITTING SHAPED FIBER OPTIC DELIVERY SYSTEM
- K102755 — CERALAS E/ 1470NM FIBER-COUPLED DIODE LASER FAMILY; CREALAS HPD MULTIWAVELENGHT 980NM/ 1470NM FIBER-COUPLED DIODE LASER
- K101712 — ENDOVASCULAR LAER VEIN SYSTEM KIT
- K100726 — CERALAS D/ 980NM FIBER-COUPLED DIODE LASER FAMILY, CERALAS E/ 980NM FIBER-COUPLED DIODE LASER FAMILY, CERALAS HPD/ 980NM
- K090164 — CERALAS MULTIWAVELENGTH 980/1470NM DIODE LASER
- K083682 — 180W CERELAS D 980NM DIODE LASER, MODEL D180
- K082225 — 15W CERALAS D 1470NM DIODE LASER, MODEL D1470
- K082263 — CERALAS E 980NM DIODE LASER, MODELS E15/980 AND E30/980
- K081015 — CERALAS D 980NM DIODE LASER, MODELS D15 AND D25
- K072682 — 50W CERALAS D 1950NM DIODE LASER
- K073063 — 15W CERALAS D 1470NM DIODE LASER
- K072779 — CERALAS D 980NM DIODE LASER, MODELS D15 AND D25
- K072106 — 150W CERALAS D 980NM DIODE LASER
- K071295 — 100W CERALAS D 980NM DIODE LASER
- K060050 — MEGABEAM SIDEFIBER FIBER OPTIC DELIVERY SYSTEM
- K050824 — 100W CERALAS D 980 LASER SYSTEM, MODEL D100
- K032863 — CERALAS D 980 DIODE LASER SYSTEM, MODELS D15, D25, D50
- K032864 — CERALAS D 810 DIODE LASER SYSTEM, MODEL D15
- K030700 — CERALAS D 10-60 810NM LASER SYSTEM WITH ENDO LASER VEIN SYSTEM KIT
- K024088 — CERALAS D 980 LASER SYSTEM WITH ENDO LASER VEIN SYSTEM KIT, MODEL: D15 AND D25
- K013691 — CERALAS D DIODE LASER SYSTEM, MODEL # D50
- K020835 — CERALAS D10-60 810NM DIODE LASER, MODELCERALAS DIO-60
- K020099 — MEGA BEAM/CERALAS NONSTERILE COLLIMATING HANDPIECE
- K013193 — MEGA BEAM/CERALAS NONSTERILE COLLIMATING HANDPIECE
- K010804 — MEGABEAM/CERALAS REUSEABLE HANDPIECE AND DISPOSABLE TIPS
- K010689 — MEGABEAM/CERALAS NON STERILE FIBER OPTIC LASER DELIVERY SYSTEMS, MODEL 200,320,400 OR 600UM
Data sourced from openFDA. This site is unofficial and independent of the FDA.