Entellus Medical, Inc.
FDA 510(k) medical device clearances.
Top product codes for Entellus Medical, Inc.
Recent clearances by Entellus Medical, Inc.
- K220027 — Audion ET dilation system
- K163435 — Entellus Medical Reinforced Anesthesia Needle
- K163509 — XprESS ENT Dilation System
- K152434 — XprESS Multi-Sinus Dilation System
- K152435 — PassAssist LED Light Fiber
- K142252 — XprESS Multi-Sinus Dilation Tool
- K141916 — PATHASSIST LED LIGHT FIBER
- K133563 — PATHASSIST LIGHT SEEKER
- K132440 — XPRESS MULTI-SINUS DILATION TOOL
- K130503 — PATHASSIST LED LIGHT FIBER
- K121943 — XPRESS MULTI-SINUS DILATION TOOL
- K121174 — XPRESS MULTI-SINUS DILATION TOOL
- K120962 — PATHASSIST LIGHT FIBER
- K120735 — PATHASSIT LIGHT SEEKER
- K113522 — PATHASSIST LIGHT SEEKER
- K112506 — XPRESS MULTI-SINUS DILATION TOOL
- K111763 — PATHASSIST LIGHT FIBER
- K110739 — ENTELLUS MEDICAL SINUS GUIDEWIRE
- K110158 — ILLUMINATING SINUS SEEKER
- K102366 — FINESS ENDOSCOPE
- K103213 — FINESS ENDOSCOPE STERILIZATION TRAY
- K102003 — XPRESS BALLOON DEVICE
- K093007 — ENTELLUS MEDICAL BALLOON DEVICE
- K091681 — FINESS SINUS TREATMENT SYSTEM (ACCESS SHEATH COMPONENT)
- K082569 — ENTELLUS MEDICAL FLEXIBLE ENDOSCOPE AND EYEPIECE
- K081542 — MODIFICATION TO ENTELLUS MEDICAL RS-SERIES SYSTEM
- K072302 — ENTELLUS MEDICAL RS-SERIES SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.