Ellex Medical Pty, Ltd.

13 FDA 510(k) medical device clearances.

Top product codes for Ellex Medical Pty, Ltd.

HQF — Ophthalmic 8 devices
GEX — General, Plastic Surgery 4 devices
IYO — Radiology 1 device

Recent clearances by Ellex Medical Pty, Ltd.

K222395 — Tango Neo, Tango Reflex Neo, Ultra Q Reflex Neo HQF · 2022-11-02
K212630 — Tango, Tango Reflex, Ultra Q, Ultra Q Reflex, Solo HQF · 2021-12-16
K190786 — Eye Prime IYO · 2019-04-11
K142398 — Integre Pro Scan Green, Integre Pro Scan Yellow, Integre Pro Scan Red-Green, Integre Pro Scan Red-Yellow HQF · 2015-07-14
K122202 — ELLEX 2RT HQF · 2013-07-01
K081565 — INTEGRE PRO, MODEL L2RY HQF · 2008-07-02
K080423 — INTEGRE, MODEL LP581 HQF · 2008-03-11
K052777 — LASEREX DUO FAMILY OF DUAL WAVELENGTH OPHTHALMIC LASERS INCLUDING MODELS INTEGRE DUO LP1RG-S, LP1RG-D GEX · 2006-03-16
K041598 — LASEREX, MODEL LP4532 HQF · 2004-10-06
K021550 — LUMENIS SELECTA DUET GEX · 2002-08-09
K003955 — LASEREX INTEGRE, MODEL LP2532 GEX · 2001-03-15
K992824 — LASEREX ND:YAG OPHTHALMIC LASER (LQ2106), ALCON ND:YAG OPHTHALMIC LASER (3000LE), LASEREX ND:YAG OPHTHALMIC LASER, MODEL GEX · 1999-11-17
K972514 — LASEREX LP1532 PHOTOCOAGULATOR HQF · 1997-10-03

Data sourced from openFDA. This site is unofficial and independent of the FDA.