Emed Technologies Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Emed Technologies Corporation - FDA 510(k) Cleared Devices
Recent clearances: Tetra (TM-20), SCIg60 Infusion System, VersaPump Infusion System
11
Total
11
Cleared
0
Denied
Emed Technologies Corporation has 11 FDA 510(k) cleared general hospital devices. Based in El Dorado Hills, US.
Latest FDA clearance: Dec 2025. Active since 2012.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Emed Technologies Corporation
11 devices
Cleared
Dec 22, 2025
Tetra (TM-20)
General Hospital
255d
Cleared
Feb 16, 2024
SCIg60 Infusion System
General Hospital
28d
Cleared
Nov 28, 2023
VersaPump Infusion System
General Hospital
243d
Cleared
Oct 20, 2022
AccuSert Needle Inserter
General Hospital
364d
Cleared
Oct 13, 2022
SCIg60 Infusion System
General Hospital
90d
Cleared
Dec 14, 2018
SCIg60 Infusion System
General Hospital
366d
Cleared
Dec 01, 2016
SCIg60 Infuser
General Hospital
142d
Cleared
May 14, 2015
SCIg60 Infuser, Infuset
General Hospital
267d
Cleared
May 15, 2014
INFUSET FLOW CONTROL EXTENSION SET
General Hospital
118d
Cleared
Apr 03, 2014
SUB-Q SUBCUTANEOUS TISSUE INFUSION SET
General Hospital
76d
Cleared
Dec 21, 2012
VERSARATE FLOW RATE CONTROLER
General Hospital
16d