Mira, Inc.
Mira, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1997.
Top product codes for Mira, Inc.
Recent clearances by Mira, Inc.
- K951728 — SCHEPENS-YOSHIDA VIDEO BINOCULAR INDIRECT OPHTHALMSCOPE
- K950806 — SOLID DILICONE IMPLANTS, SDILICONE SPONGE IMPLANTS
- K941495 — RETURN PATH DIATHERMY HANDLE
- K933527 — MODIFICATION OF ANTERIOR SEGMENT ELECTRODES
- K923629 — OPHTHALMIC TRICHIASIS PROBE
- K894248 — CONVERTER SYSTEM
- K891601 — POWER OPERATED AND CONTROLLED VITREOUS SCISSORS
- K890448 — LIGHT SOURCE, ENDOSCOP, XENON ARC
- K863246 — MIRALITE
- K863591 — ENDOPHOTOCOAGULATION PROBE
- K855105 — SIMMONS SHELL
- K854869 — INTRAOCULAR FORCEPS & SCISSORS
- K855215 — AIR/FLUID EXCHANGE SYSTEM
- K854870 — INTRAOCULAR ELECTROMAGNET
- K854872 — VFI/VFE SYSTEM II
- K854868 — I/A - VFE SYSTEM II
- K854871 — MICRO SURGICAL SYSTEM
- K854873 — INTRAOCULAR PRESSURE REDUCER
- K853890 — OPHTHALMIC LASER PHOTOCOAGULATOR
- K854288 — OPHALMIC LASER PHOTOCOAGULATOR
- K843345 — AGL400 ARGON LASER SYSTEM-KRL500 KRYPTON
Data sourced from openFDA. This site is unofficial and independent of the FDA.