FDA 510(k) Applications Submitted by TRIMED, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K102785	09/27/2010	TRIMED RADIOCARPAL FUSION SYSTEM	TRIMED, INC.
K190166	01/31/2019	TriMed Nitinol Staple System	TriMed, Inc.
K220650	03/07/2022	TriMed Ripcord Device	TriMed, Inc.
K230749	03/17/2023	TriMed Threaded Intramedullary Nail System	TriMed, Inc.
K230805	03/23/2023	TriMed Clavicle Fixation System	TriMed, Inc.
K211783	06/09/2021	TriMed Threaded Intramedullary Nail System	TriMed, Inc.
K222637	08/31/2022	TriMed Wrist Fixation System 3	TriMed, Inc.
K192696	09/26/2019	TriMed ASET Foot Plating System	TriMed, Inc.
K111266	05/04/2011	EASYLOCK OSTEOSYSTEM	TRIMED, INC.
K112509	08/30/2011	TRIMED CLAVICLE FIXATION SYSTEM	TRIMED, INC.
K112794	09/26/2011	EOS SMALL BONE FIXATION SYSTEM	TRIMED, INC.
K060041	01/06/2006	TRIMED BONE PLATES	TRIMED, INC.
K050681	03/16/2005	OMNITECH SYSTEM & EASY LOCK OSTEOSYSTEM WITH XTREMITIES PLATES	TRIMED, INC.
K091156	04/21/2009	TRIMED STERILE PRODUCT	TRIMED, INC.
K081348	05/14/2008	TENODESIS CROSS SCREW, INTERFERENCE SCREW, SUTURE BEAD	TRIMED, INC.
K101375	05/17/2010	TRIMED X-FIX	TRIMED, INC.
K071876	07/06/2007	CROSS.BONE	TRIMED, INC.
K043263	11/24/2004	TRIMED OSTEOTOMY PLATE	TRIMED, INC.
K093676	11/27/2009	OMNITECH LARGE, TRIMED COMPRESSION SCREW	TRIMED, INC.
K151735	06/26/2015	TriMed Humeral Supracondylar Fixation System	TriMed, Inc.