Staar Surgical Co. is one of 13119 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Staar Surgical Co. - FDA 510(k) Cleared Devices
Recent clearances: EPIPHANY INJECTION SYSTEM, MICROSTAAR INDIGO INJECTOR FOAM TIP SYSTEM, MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM
22
Total
22
Cleared
0
Denied
Staar Surgical Co. has 22 FDA 510(k) cleared ophthalmic devices. Based in Mchenry, US.
Historical record: 22 cleared submissions from 1983 to 2009.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Staar Surgical Co.
22 devices
Cleared
Jun 09, 2009
EPIPHANY INJECTION SYSTEM
Ophthalmic
138d
Cleared
Mar 13, 2008
MICROSTAAR INDIGO INJECTOR FOAM TIP SYSTEM
Ophthalmic
84d
Cleared
Mar 13, 2008
MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM
Ophthalmic
84d
Cleared
Jun 10, 2004
RE-USEABLE MICROSTAAR INJECTOR, MSI-S
Ophthalmic
310d
Cleared
May 16, 2002
SURGE-FREE ASPIRATION ADAPTER
Ophthalmic
71d
Cleared
Dec 04, 1998
DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)
Ophthalmic
87d
Cleared
Sep 11, 1998
FOAM TIP INJECTOR
Ophthalmic
200d
Cleared
Dec 21, 1995
MICROSTAAR INJECTOR MODELS MSI-TD & MSI-PD (MODIFICATION)
Ophthalmic
87d
Cleared
Dec 18, 1991
SOFTRANS INJECTOR
Ophthalmic
125d
Cleared
Feb 17, 1989
STAAR PHACO XL SMALL INCISION SYSTEM
Ophthalmic
129d
Cleared
Mar 30, 1988
MOLTENO VALVE SETON
Ophthalmic
111d
Cleared
Nov 13, 1986
FAULKNER FORCEPS
Ophthalmic
24d