FDA 510(k) Applications Submitted by ORLY MAOR

FDA 510(k) Number Submission Date Device Name Applicant
K020127 01/15/2002 SMARTFLOW PULSE TRANSMISSION COEFFICIENT FLORENCE MEDICAL LTD.
K110159 01/19/2011 ACTIVECARE SFT MEDICAL COMPRESSION SYSTEMS (DBN) LTD.
K030192 01/21/2003 DUET SYSTEM BIOVIEW LTD.
K050356 02/14/2005 COMPRESSION ANASTOMOSIS RING (CAR) NITI MEDICAL TECHNOLOGIES LTD.
K130775 03/20/2013 DUET SYSTEM BIOVIEW LTD.
K041751 06/29/2004 COMPRESSION ANASTOMOSIS CLIP (CAC) NITI MEDICAL TECHNOLOGIES LTD.
K062008 07/17/2006 ENDO CAR COMPRESSION ANASTOMOSIS RING (CAR) NITI MEDICAL TECHNOLOGIES LTD.
K202483 08/28/2020 MyHomeDoc MyHomeDoc Ltd.
K042492 09/14/2004 HAND STC, MODEL 60MM NITI MEDICAL TECHNOLOGIES LTD.
K023161 09/23/2002 SMARTSTEP SYSTEM ANDANTE MEDICAL DEVICE, LTD.
K033324 10/15/2003 COMPRESSION ANASTOMOSIS CLIP (CAC) NITI MEDICAL TECHNOLOGIES LTD.
K043115 11/10/2004 LAPAROSCOPIC COMPRESSION ANASTOMOSIS CLIP (LAPCAC) NITI MEDICAL TECHNOLOGIES LTD.
K153519 12/08/2015 DReal CAREVATURE MEDICAL LTD
K223785 12/16/2022 N9+ Nonagon Ltd.


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