FDA 510(k) Applications Submitted by FCI OPHTHALMICS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K980816 |
03/03/1998 |
RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES |
FCI OPHTHALMICS, INC. |
| K980822 |
03/03/1998 |
TITANIUM PEG SYSTEM |
FCI OPHTHALMICS, INC. |
| K991238 |
04/12/1999 |
FCI CRAWFORD PROBE INTUBATION SETS |
FCI OPHTHALMICS, INC. |
| K961909 |
05/16/1996 |
READY-SET PUNCTAL PLUGS |
FCI OPHTHALMICS, INC. |
| K992294 |
07/07/1999 |
BIOCERAMIC ORBITAL IMPLANT |
FCI OPHTHALMICS, INC. |
| K963219 |
08/16/1996 |
RETINAL DETACHMENT IMPLANTS; INCLUDING BANS, STRIPS, TIRES, SLEEVES, CORDS AND SPONGES |
FCI OPHTHALMICS, INC. |
| K964774 |
10/22/1996 |
PUNCTUM PLUGS & READY-SET PUNCTAL PLUGS |
FCI OPHTHALMICS, INC. |
| K030054 |
01/06/2003 |
DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSES |
FCI OPHTHALMICS, INC. |
| K061398 |
05/19/2006 |
SNUG PLUG PUNCTUM PLUG |
FCI OPHTHALMICS, INC. |
| K061404 |
05/19/2006 |
MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE |
FCI OPHTHALMICS, INC. |
| K023400 |
10/09/2002 |
FCI MESH WRAPPED BIOCERAMIC ORBITAL IMPLANT |
FCI OPHTHALMICS, INC. |
| K023758 |
11/08/2002 |
BECKER TRANSNASAL LACRIMAL (INTUBATION SETS) |
FCI OPHTHALMICS, INC. |
| K041869 |
07/09/2004 |
SELF RETAINING BICANALICULUS INTUBATION SET |
FCI OPHTHALMICS, INC. |
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