Fci Ophthalmics, Inc.
Fci Ophthalmics, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2006.
Top product codes for Fci Ophthalmics, Inc.
Recent clearances by Fci Ophthalmics, Inc.
- K061404 — MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
- K061398 — SNUG PLUG PUNCTUM PLUG
- K041869 — SELF RETAINING BICANALICULUS INTUBATION SET
- K023758 — BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)
- K023400 — FCI MESH WRAPPED BIOCERAMIC ORBITAL IMPLANT
- K030054 — DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSES
- K992294 — BIOCERAMIC ORBITAL IMPLANT
- K991238 — FCI CRAWFORD PROBE INTUBATION SETS
- K980816 — RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES
- K980822 — TITANIUM PEG SYSTEM
- K964774 — PUNCTUM PLUGS & READY-SET PUNCTAL PLUGS
- K963219 — RETINAL DETACHMENT IMPLANTS; INCLUDING BANS, STRIPS, TIRES, SLEEVES, CORDS AND SPONGES
- K961909 — READY-SET PUNCTAL PLUGS
Data sourced from openFDA. This site is unofficial and independent of the FDA.