Medicel AG - FDA 510(k) Cleared Devices
Recent clearances: ACCUJECT Injector Set 2.1-1P (LP604590), Accuject Refra Injector AR2900
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Medicel AG Ophthalmic ✕
6 devices
Cleared
Sep 16, 2025
ACCUJECT Injector Set 2.1-1P (LP604590)
Ophthalmic
35d
Cleared
Sep 19, 2023
Accuject Refra Injector AR2900
Ophthalmic
153d
Cleared
Aug 09, 2010
VISIAN NANOPOINT 2.0 INJECTOR MODEL LP604430
Ophthalmic
109d
Cleared
Jul 28, 2009
NAVIJECT SUB2-1P, MODEL: LP604430
Ophthalmic
22d
Cleared
Nov 01, 2007
IOL INJECTOR SET
Ophthalmic
234d
Cleared
Jun 17, 2004
MULTIJECT INJECTOR AND MICROGLIDE CARTRIDGE
Ophthalmic
78d