Iridex Corp
Iridex Corp holds FDA 510(k) medical device clearances, first cleared 1998, most recent 2012.
Top product codes for Iridex Corp
Recent clearances by Iridex Corp
- K121475 — TXCELL SCANNING LASER DELIVERY SYSTEM
- K071687 — FAMILI OF IRIDEX IQ LASER SYSTEMS
- K062074 — IRIDEX WIRELESS FOOTSWITCH
- K062369 — IRIDEX OCULIGHT TX
- K060905 — IRIDEX OTOPROBE LONG AND SHORT ANGLES, P/N 14310-1 AND 14320-1
- K050562 — OCULIGHT GL/GLX
- K040209 — IRIS MEDICAL IQ 810 PHOTOCOAGULATOR
- K031665 — IRIS MEDICAL OCULIGHT GL/GLX LASER SYSTEMS
- K022228 — FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES
- K020849 — APEX 800 LASER SYSTEM, MODEL APEX 800
- K020374 — OCULIGHT SL/SLX
- K992298 — IRIDERM, MODEL APEX 800
- K982031 — OCULIGHT GL WITH THE DERMATOLOGY HANDPIECE
Data sourced from openFDA. This site is unofficial and independent of the FDA.