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510(k) K232151

Device
Dynamic TiBase
Applicant
Talladium España, SL
510(k) number
K232151
Product code
NHA
Decision
Substantially Equivalent (SESE)
Decision date
2023-10-17
Date received
2023-07-19
Regulation
872.3630
Classification name
Abutment, Implant, Dental, Endosseous
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Xavier Soca Filella
Address
Virginia Woolf, 17 Lleida ES 25005 25005

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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510(k), Device, Applicant table
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K251515Solidex® Ti-Links and ScrewsCreoDent Hudson Valley2026-02-10
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K243732Multi-Unit DAS SystemTalladium España, SL2026-01-29
K253315Straumann Variobase Abutments XC for Bridge/BarInstitut Straumann AG2026-01-22
K253253IPDmilled BlanksImplant Protesis Dental 2004, S.L.2026-01-22
K252727Neodent InLab Validated WorkflowJJGC Indústria e Comércio de Materiais Dentários S.A.2026-01-07
K253341Custom Abutments ASMedentika GmbH2025-12-23
K253312OrangeCAD Med AbutmentsOrangecad Med GmbH2025-12-23
K252320SIMDA AbutmentsSimda Co., Ltd.2025-12-18