Mira, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SCHEPENS-YOSHIDA VIDEO BINOCULAR INDIRECT OPHTHALMSCOPE, SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTS, RETURN PATH DIATHERMY HANDLE
21
Total
21
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mira, Inc. Ophthalmic ✕
17 devices
Cleared
Mar 19, 1997
SCHEPENS-YOSHIDA VIDEO BINOCULAR INDIRECT OPHTHALMSCOPE
Ophthalmic
706d
Cleared
Jun 05, 1996
SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTS
Ophthalmic
469d
Cleared
Jul 15, 1994
RETURN PATH DIATHERMY HANDLE
Ophthalmic
109d
Cleared
Oct 19, 1992
OPHTHALMIC TRICHIASIS PROBE
Ophthalmic
90d
Cleared
Feb 27, 1990
CONVERTER SYSTEM
Ophthalmic
251d
Cleared
May 23, 1989
POWER OPERATED AND CONTROLLED VITREOUS SCISSORS
Ophthalmic
64d
Cleared
Oct 31, 1986
MIRALITE
Ophthalmic
70d
Cleared
Oct 10, 1986
ENDOPHOTOCOAGULATION PROBE
Ophthalmic
25d
Cleared
Mar 31, 1986
SIMMONS SHELL
Ophthalmic
98d
Cleared
Mar 05, 1986
INTRAOCULAR FORCEPS & SCISSORS
Ophthalmic
91d
Cleared
Feb 19, 1986
INTRAOCULAR ELECTROMAGNET
Ophthalmic
77d
Cleared
Feb 13, 1986
VFI/VFE SYSTEM II
Ophthalmic
71d
Cleared
Feb 07, 1986
I/A - VFE SYSTEM II
Ophthalmic
65d
Cleared
Feb 07, 1986
MICRO SURGICAL SYSTEM
Ophthalmic
65d
Cleared
Nov 12, 1985
OPHTHALMIC LASER PHOTOCOAGULATOR
Ophthalmic
54d
Cleared
Nov 12, 1985
OPHALMIC LASER PHOTOCOAGULATOR
Ophthalmic
18d
Cleared
Nov 06, 1984
AGL400 ARGON LASER SYSTEM-KRL500 KRYPTON
Ophthalmic
71d