Simplivia Healthcare , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Simplivia Healthcare , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor, Chemfort Female Luer Lock Adaptor, Chemfort® Catheter Adaptor
6
Total
6
Cleared
0
Denied
Simplivia Healthcare , Ltd. has 6 FDA 510(k) cleared medical devices. Based in Kiryat Shmona, IL.
Latest FDA clearance: Oct 2025. Active since 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Simplivia Healthcare , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Donawa Lifescience Consulting as regulatory consultant.
FDA 510(k) Regulatory Record - Simplivia Healthcare , Ltd.
6 devices
Cleared
Oct 21, 2025
Chemfort® 28-day 20 mm Vial Adaptor and 13 mm Convertor
General Hospital
29d
Cleared
Aug 05, 2025
Chemfort Female Luer Lock Adaptor
General Hospital
90d
Cleared
Aug 02, 2023
Chemfort® Catheter Adaptor
General Hospital
90d
Cleared
Sep 23, 2021
OnGuard2 Chemfort Closed Administration (CADM)
General Hospital
197d
Cleared
Feb 25, 2021
TEVADAPTOR Bag Adaptor LL, TEVADAPTOR Bag Adaptor LL with ULTRASITE,...
General Hospital
302d
Cleared
May 07, 2020
Chemfort CSTD
General Hospital
213d