ClearanceBrief
Company ยท US

Addent, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2019. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EAZLight, Operating, Dental2
NXVDiagnostic Light, Soft Tissue Detector2
EBZActivator, Ultraviolet, For Polymerization1
NTKLight Transmission Caries Detector1
QGOComposite Resin Warmer1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 29, 2019K182017Compex HD
Addent, Inc.
QGO
Jul 24, 2012K121282MICROLUX/DL MICROLUX/BLU BIO/SCREEN
Addent, Inc.
NXV
Jan 23, 2009K082668BIO-SCREEN
Addent, Inc.
NXV
Nov 19, 2007K072309MICROLUX/BLU
Addent, Inc.
EAZ
Feb 8, 2007K062961MICROLUX TRANSILLUMINATOR
Addent, Inc.
NTK
Jun 23, 2006K061395CALSET COMPOSITE HEATER
Addent, Inc.
EBZ
Apr 4, 2005K041614MICROLUX DL
Addent, Inc.
EAZ

Latest recalls

DateFirm and productCodeLinked 510(k)
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