Syneron Medical, Ltd.
FDA 510(k) medical device clearances.
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.