ClearanceBrief
Company ยท US

Emed Technologies Corporation

FDA 510(k) clearances and medical device recalls filed under this name, 2012 to 2025. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
PKPImmunoglobulin G (Igg) Infusion System7
FPASet, Administration, Intravascular3
KZHIntroducer, Syringe Needle1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Dec 22, 2025K251105Tetra (TM-20); Tetra (TM-50)
Emed Technologies Corporation
PKP
Feb 16, 2024K240148SCIg60 Infusion System
Emed Technologies Corporation
PKP
Nov 28, 2023K230883VersaPump Infusion System
Emed Technologies Corporation
PKP
Oct 20, 2022K213429AccuSert Needle Inserter
Emed Technologies Corporation
KZH
Oct 13, 2022K222087SCIg60 Infusion System
Emed Technologies Corporation
PKP
Dec 14, 2018K173783SCIg60 Infusion System
Emed Technologies Corporation
PKP
Dec 1, 2016K161906SCIg60 Infuser
Emed Technologies Corporation
PKP
May 14, 2015K142319SCIg60 Infuser, Infuset
Emed Technologies Corporation
PKP
May 15, 2014K140133INFUSET FLOW CONTROL EXTENSION SET
Emed Technologies Corporation
FPA
Apr 3, 2014K140131SUB-Q SUBCUTANEOUS TISSUE INFUSION SET
Emed Technologies Corporation
FPA
Dec 21, 2012K123729VERSARATE FLOW RATE CONTROLER
Emed Technologies Corporation
FPA

Latest recalls

DateFirm and productCodeLinked 510(k)
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