Ellex Medical Pty, Ltd. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Ellex Medical Pty, Ltd. has 13 FDA 510(k) cleared medical devices. Based in Adelaide, South Australia, AU.
Last cleared in 2022. Active since 1997. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Ellex Medical Pty, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Ellex Medical Pty, Ltd.
13 devices
Cleared
Nov 02, 2022
Tango Neo, Tango Reflex Neo, Ultra Q Reflex Neo
Ophthalmic
86d
Cleared
Dec 16, 2021
Tango, Tango Reflex, Ultra Q, Ultra Q Reflex, Solo
Ophthalmic
119d
Cleared
Apr 11, 2019
Eye Prime
Radiology
15d
Cleared
Jul 14, 2015
Integre Pro Scan Green, Integre Pro Scan Yellow, Integre Pro Scan Red-Green,...
Ophthalmic
321d
Cleared
Jul 01, 2013
ELLEX 2RT
Ophthalmic
341d
Cleared
Jul 02, 2008
INTEGRE PRO, MODEL L2RY
Ophthalmic
28d
Cleared
Mar 11, 2008
INTEGRE, MODEL LP581
Ophthalmic
25d
Cleared
Mar 16, 2006
LASEREX DUO FAMILY OF DUAL WAVELENGTH OPHTHALMIC LASERS INCLUDING MODELS...
General & Plastic Surgery
164d
Cleared
Oct 06, 2004
LASEREX, MODEL LP4532
Ophthalmic
114d
Cleared
Aug 09, 2002
LUMENIS SELECTA DUET
General & Plastic Surgery
88d
Cleared
Mar 15, 2001
LASEREX INTEGRE, MODEL LP2532
General & Plastic Surgery
84d
Cleared
Nov 17, 1999
LASEREX ND:YAG OPHTHALMIC LASER (LQ2106), ALCON ND:YAG OPHTHALMIC LASER...
General & Plastic Surgery
86d