FDA 510(k) Applications Submitted by Implant Direct Sybron Manufacturing LLC

FDA 510(k) Number	Submission Date	Device Name	Applicant
K143011	10/20/2014	2014 InterActive/SwishActive System	Implant Direct Sybron Manufacturing LLC
K153509	12/07/2015	GPS Angled Abutment	IMPLANT DIRECT SYBRON MANUFACTURING LLC
K130572	03/04/2013	INTERACTIVE/ SWISHPLUS2 IMPLANT SYSTEM	IMPLANT DIRECT SYBRON MANUFACTURING LLC
K131097	04/18/2013	LEGACY3 6MM LENGTH IMPLANTS	IMPLANT DIRECT SYBRON MANUFACTURING LLC
K181359	05/22/2018	InterActive SMARTBase Abutments	Implant Direct Sybron Manufacturing LLC
K191458	05/31/2019	Legacy SMARTBase Abutments	Implant Direct Sybron Manufacturing LLC
K222211	07/25/2022	Implant Direct Dental Implant Systems Portfolio - MR Conditional	Implant Direct Sybron Manufacturing LLC
K223535	11/23/2022	SMARTbase Abutment System	Implant Direct Sybron Manufacturing LLC