Fci Ophthalmics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fci Ophthalmics, Inc. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Fci Ophthalmics, Inc. has 13 FDA 510(k) cleared ophthalmic devices. Based in Centercille, US.
Historical record: 13 cleared submissions from 1996 to 2006.
Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fci Ophthalmics, Inc.
13 devices
Cleared
Aug 07, 2006
MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE
Ophthalmic
80d
Cleared
Jul 11, 2006
SNUG PLUG PUNCTUM PLUG
Ophthalmic
53d
Cleared
Nov 18, 2004
SELF RETAINING BICANALICULUS INTUBATION SET
Ophthalmic
132d
Cleared
Sep 17, 2003
BECKER TRANSNASAL LACRIMAL (INTUBATION SETS)
Ophthalmic
313d
Cleared
Aug 22, 2003
FCI MESH WRAPPED BIOCERAMIC ORBITAL IMPLANT
Ophthalmic
317d
Cleared
Feb 26, 2003
DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSES
Ophthalmic
51d
Cleared
Apr 19, 2000
BIOCERAMIC ORBITAL IMPLANT
Ophthalmic
287d
Cleared
Jul 08, 1999
FCI CRAWFORD PROBE INTUBATION SETS
Ophthalmic
87d
Cleared
Sep 18, 1998
RETINAL DETACHMENT IMPLANTS, INCLUDING BANDS, STRIPS (RAILS) AND SPONGES
Ophthalmic
199d
Cleared
Jul 09, 1998
TITANIUM PEG SYSTEM
Ophthalmic
128d
Cleared
Dec 20, 1996
PUNCTUM PLUGS & READY-SET PUNCTAL PLUGS
Ophthalmic
59d
Cleared
Oct 28, 1996
RETINAL DETACHMENT IMPLANTS
Ophthalmic
73d
Cleared
Jul 25, 1996
READY-SET PUNCTAL PLUGS
Ophthalmic
70d