FDA 510(k) Applications Submitted by JOHN SU

FDA 510(k) Number Submission Date Device Name Applicant
K132245 07/18/2013 AJAX DENTAL UNIT PRO DENTAL SERVICES LLC.
K140399 02/18/2014 EBM IDO VIEWER EBM TECHNOLOGIES USA, LLC
K202292 08/12/2020 UDE EBM Technologies Inc.
K162285 08/15/2016 EBM iDO Viewer 1.2.1 EBM Technologies Incorporated
K142514 09/08/2014 UniWeb 8.0 EBM Technologies Incorporated
K180364 02/12/2018 HD LifeSciences Cervical IBFD System HD LifeSciences LLC
K200541 03/03/2020 HiveÖ Stand-alone Anterior Lumbar Interbody System HD LifeSciences LLC
K091638 06/04/2009 DORADO WIDE INTERVERTEBRAL BODY CAGE, MODELS: IM2010-IM2031 SPINEFRONTIER, INC.
K102020 07/19/2010 VEGA SPAN SPINOUS PROCESS PLATE SYSTEM SPINEFRONTIER, INC.
K092420 08/06/2009 KRD1 PEDICLE SCREW SYSTEM SPINEFRONTIER, INC.
K092815 09/14/2009 S-LIF INTERVERTEBRAL BODY FUSION DEVICE SPINEFRONTIER, INC.
K213266 09/30/2021 Inspan ScrewLES Fusion System LESpine Innovations, LLC
K093776 12/08/2009 INDUS ANTERIOR CERVICAL PLATE SYSTEM SPINEFRONTIER, INC.
K222127 07/18/2022 Soft Palate Elevator The TMJ Clinic, PC.
K972325 06/23/1997 PULSEMASTER 1000 ST DENTAL LASER SYSTEM AMERICAN DENTAL TECHNOLOGIES, INC.
K984486 12/17/1998 PULSEMASTER DENTAL LASER SYSTEM AMERICAN DENTAL TECHNOLOGIES, INC.


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