Endymed Medical, Ltd. is one of 472 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Endymed Medical, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: EndyMed PRO MAX, PURE Laser, EndyGel
8
Total
7
Cleared
1
Denied
Endymed Medical, Ltd. has 7 FDA 510(k) cleared medical devices. Based in Binyamina, IL.
Latest FDA clearance: Jun 2025. Active since 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Endymed Medical, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qsite as regulatory consultant.
FDA 510(k) Regulatory Record - Endymed Medical, Ltd.
8 devices
Cleared
Jun 10, 2025
EndyMed PRO MAX
General & Plastic Surgery
257d
Cleared
Oct 07, 2022
PURE Laser
General & Plastic Surgery
63d
Cleared
Feb 07, 2017
EndyGel
Neurology
231d
Cleared
Aug 01, 2016
EndyMed Contour Handpiece
General & Plastic Surgery
95d
Not Cleared
Dec 18, 2015
Newa Skin Therapy System
General & Plastic Surgery
336d
Cleared
Mar 13, 2014
INTENSIF
General & Plastic Surgery
379d
Cleared
May 08, 2012
GLOW BY ENDYMED
General & Plastic Surgery
77d
Cleared
Feb 17, 2011
FRACTIONAL SKIN RESURFACING (FSR) APPLICATOR
General & Plastic Surgery
261d