ClearanceBrief
Company ยท US

Valeritas, Incorporated

FDA 510(k) clearances and medical device recalls filed under this name, 2010 to 2011. Name variants (Inc, Corp, punctuation) are merged.

2510(k) clearances (0 in 12 months)
5recalls (0 in 12 months)
5recalls that name a 510(k)

Product codes

CodeDeviceRecords
LZGPump, Infusion, Insulin7

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Feb 23, 2011K103825V-GO INSULIN DELIVERY SYSTEM
Valeritas, Inc.
LZG
Dec 1, 2010K100504V-GO DISPOSABLE INSULIN DELIVERY DEVICE, MODEL# V-GO 20, V-GO 30, V-GO40
Valeritas, LLC
LZG

Latest recalls

DateFirm and productCodeLinked 510(k)
Jul 3, 2019Valeritas, Incorporated
DEMO No Needle Corrugated Carton 30 U/D, Part Number 2568-02
Terminated		 LZGK103825
Jul 3, 2019Valeritas, Incorporated
DEMO No Needle Corrugated Carton 20 U/D, Part Number 2568-03
Terminated		 LZGK103825
Jul 3, 2019Valeritas, Incorporated
DEMO No Needle Corrugated Carton 40 U/D, Part Number 2260-01
Terminated		 LZGK103825
Jul 3, 2019Valeritas, Incorporated
DEMO No Needle Corrugated Carton 30 U/D, Part Number 2260-02
Terminated		 LZGK103825
Jul 3, 2019Valeritas, Incorporated
DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03
Terminated		 LZGK103825
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