Fci Ophthalmics, Inc.
FDA 510(k) medical device clearances.
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.