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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