Ellex Medical Pty, Ltd.
Ellex Medical Pty, Ltd. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2022, with 1 FDA device recall on record.
Top product codes for Ellex Medical Pty, Ltd.
FDA recalls by Ellex Medical Pty, Ltd.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Ellex Medical Pty, Ltd.
- K222395 — Tango Neo, Tango Reflex Neo, Ultra Q Reflex Neo
- K212630 — Tango, Tango Reflex, Ultra Q, Ultra Q Reflex, Solo
- K190786 — Eye Prime
- K142398 — Integre Pro Scan Green, Integre Pro Scan Yellow, Integre Pro Scan Red-Green, Integre Pro Scan Red-Yellow
- K122202 — ELLEX 2RT
- K081565 — INTEGRE PRO, MODEL L2RY
- K080423 — INTEGRE, MODEL LP581
- K052777 — LASEREX DUO FAMILY OF DUAL WAVELENGTH OPHTHALMIC LASERS INCLUDING MODELS INTEGRE DUO LP1RG-S, LP1RG-D
- K041598 — LASEREX, MODEL LP4532
- K021550 — LUMENIS SELECTA DUET
- K003955 — LASEREX INTEGRE, MODEL LP2532
- K992824 — LASEREX ND:YAG OPHTHALMIC LASER (LQ2106), ALCON ND:YAG OPHTHALMIC LASER (3000LE), LASEREX ND:YAG OPHTHALMIC LASER, MODEL
- K972514 — LASEREX LP1532 PHOTOCOAGULATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.