FDA 510(k) Applications Submitted by Shlomi Dines

FDA 510(k) Number Submission Date Device Name Applicant
K230058 01/09/2023 Bladeless Trocar û Artemis Lap Cannula T.A.G. Medical Products Corporation, Ltd
K070235 01/25/2007 BODYGUARD PAIN MANAGER INFUSION SYSTEM CAESAREA MEDICAL ELECTRONICS LTD.
K190125 01/28/2019 FiberStitch Implant, Curved with two Polyester Implants and 2-0 FiberWire, FiberStitch Implant, Straight with two Polyester Implants and 2-0 FiberWire T.A.G. Medical Products Corporation, Ltd
K100400 02/16/2010 PRESTODR PORTABLE CMT MEDICAL TECHNOLOGIES, LTD.
K210498 02/22/2021 Betta Link Knotless Implant System T.A.G. Medical Products Corporation, Ltd
K070718 03/14/2007 MODIFICATION TO: BODYGUARD INFUSION SYSTEM CAESAREA MEDICAL ELECTRONICS LTD.
K110849 03/28/2011 PRESTODR 4143 CMT MEDICAL TECHNOLOGIES, LTD.
K061325 05/11/2006 BODYGAURD PAIN MANAGER INFUSION SYSTEM CAESAREA MEDICAL ELECTRONICS LTD.
K231400 05/15/2023 Bladeless Trocar û Artemis Lap Cannula T.A.G. Medical Products Corporation, Ltd
K221731 06/15/2022 FiberStitch Implant, Curved with two Polyester Implants and 2-0 FiberWire, FiberStitch Implant, Straight with two Polyester Implants and 2-0 FiberWire T.A.G. Medical Products Corporation, Ltd
K202178 08/04/2020 VersaLoop Anchor System T.A.G. Medical Products Corporation, Ltd
K103038 10/14/2010 DUET DRF CMT MEDICAL TECHNOLOGIES, LTD.


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