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TMJ Solutions, LLC

US

Last updated September 17, 2026

Information

Country
US
Address
6059 King Drive, San Buenaventura, CA, 93003
Website
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LinkedIn
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Facebook
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Email
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Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
3001237463
DUNS Number
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Catalogue (96)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2012
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0100
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2312
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2014
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0110
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2314
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System YYMMDDNNNNRM
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0100
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2310
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2008
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2308
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0130
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2312
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0510
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2010
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2308
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2312
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2308
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0300
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System CHG010AM
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0120
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System CHG020
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2005
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2310
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2006
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System CHG026
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2008
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2314
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2316
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System CHG024
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2310
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2016
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2308
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2314
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System TYY-NNNNRM
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2316
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System YYMMDDNNNNM
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2306
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0500
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0200
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System YYMMDDNNNNLM
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0110
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System 60-0200
FDA UDI
Class IActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2005
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 61-2306
FDA UDI
Class IIIActive
Patient-Fitted TMJ Reconstructive Prosthesis System 65-2006
FDA UDI
Class IIIActive

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FDA Recalls (3)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Oct 13, 2025Z-0488-2026—open, classified

Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position.

Jul 24, 2024Z-3264-2024—open, classified

Patient-fitted temporomandibular (TMJ) prothesis contained incorrect components, SterileEO

Mar 12, 2018Z-1444-2018—terminated

This device was mislabeled and is not the correct component for this patient.