Syneron Medical, Ltd.
Syneron Medical, Ltd. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2017.
Top product codes for Syneron Medical, Ltd.
Recent clearances by Syneron Medical, Ltd.
- K170370 — ULTRASHAPE POWER SYSTEM
- K163415 — SlimShape System
- K162163 — UltraShape System
- K161952 — UltraShape System
- K160896 — ULTRASHAPE POWER SYSTEM
- K151655 — CO2RE System
- K141507 — TWO SKIN TREATMENT SYSTEM
- K141708 — ULTRASHAPE SYSTEM
- K133238 — CONTOUR I V3.1 SYSTEM
- K120510 — TRANSCEND
- K121598 — ME HAIR2GO
- K122579 — VELASHAPE
- K101321 — EMATRIX CO2
- K090025 — MATRIX RF APPLICATOR
- K073572 — MATRIX RF APPLICATOR
- K073715 — ELIPO
- K071872 — VELASHAPE
- K070092 — MODIFICATION TO VELASMOOTH, SHAPER
- K053616 — POLARIS WR, ST APPLICATOR
- K052324 — POLARIS LV, LVA APPLICATOR
- K050397 — VELASMOOTH, SHAPER
- K050796 — AURORA DS, DS APPLICATOR
- K050452 — AURORA SR AND SRA APPLICATOR
- K041959 — POLARIS DS/COMET
- K041969 — AURORA DS
- K032514 — AC APPLICATOR, AURORA AC
- K033586 — MODIFICATION TO AURORA DS
- K031671 — POLARIS WR
- K031489 — PITANGA
- K031988 — AURORA DS
- K031993 — AURORA SR
- K030186 — POLRIS LV
- K024064 — POLARIS DS
- K022266 — AURORA SR
- K021149 — AURORA DS
Data sourced from openFDA. This site is unofficial and independent of the FDA.