ClearanceBrief
Company ยท US

Convergent Dental, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2013 to 2022. Name variants (Inc, Corp, punctuation) are merged.

4510(k) clearances (0 in 12 months)
2recalls (0 in 12 months)
2recalls that name a 510(k)

Product codes

CodeDeviceRecords
GEXPowered Laser Surgical Instrument4
NVKLaser, Dental, Soft Tissue2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 14, 2022K221761Solea
Convergent Dental, Inc.
NVK
Sep 23, 2015K151306Solea
Convergent Dental, Inc.
GEX
Jul 12, 2013K130420SOLEA
Convergent Dental, Inc.
GEX
Feb 11, 2013K123494SOLEA
Convergent Dental, Inc.
GEX

Latest recalls

DateFirm and productCodeLinked 510(k)
Nov 17, 2023Convergent Dental
Solea Models 2.0 and 3.0 Laser Surgical Instrument, Foot Pedal assembly SUB-00434 with foot pedal CUS-00226 Rev. K reworked
Open, Classified
NVKK221761
Oct 22, 2013Convergent Dental
Solea 1.0 Laser Surgical instrument for use in general and plastic surgery and dermatology.
Terminated
GEXK123494
K130420
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