Entellus Medical, Inc.
Entellus Medical, Inc. holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2022.
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.