FDA 510(k) Applications Submitted by HILLARD W WELCH

FDA 510(k) Number	Submission Date	Device Name	Applicant
K030054	01/06/2003	DISPOSABLE VITRECTOMY SETS, DISPOSABLE VIRECTOMY LENSES	FCI OPHTHALMICS, INC.
K110554	02/28/2011	BIOCERAMIC ORBITAL IMPLANT, ORBTEX	CERAMISYS LTD.
K980840	03/04/1998	LOKKI DT	HILLARD W. WELCH
K001125	04/07/2000	GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING	GEUDER GMBH
K961658	04/29/1996	MEGATRON OPHTHALMIC SURGICAL SYSTEM	INTL. OPHTHALMIC INDUSTRIES CORP.
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.
K994028	11/26/1999	FLIPO XENON CURING LIGHT	LOKKI
K974603	12/10/1997	PLAQUAGRAFE, AGRAFE P4V	ATLAS TECHNOLOGY
K103820	12/30/2010	REPROBONE DENTAL GRAFTING MATERIAL	CERAMISYS LTD
K024374	12/31/2002	RMO PLASMA CURING LIGHT	LOKKI LASERS MEDICAUX