Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CEREC Cercon 4D™ Abutment Blocks, CEREC Cercon 4D™ Abutment System

K-Number: K234018 · 2024-05-07

ApplicantDentsply Sirona
Decision Date2024-05-07
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CEREC Cercon 4D™ Abutment Blocks, CEREC Cercon 4D™ Abutment System is the device name listed in this FDA 510(k) record. The listed applicant is Dentsply Sirona. It received FDA 510(k) clearance on 2024-05-07 under 510(k) number K234018. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CEREC Cercon 4D™ Abutment Blocks, CEREC Cercon 4D™ Abutment System?

CEREC Cercon 4D™ Abutment Blocks, CEREC Cercon 4D™ Abutment System is a medical device that received FDA 510(k) clearance on 2024-05-07. The listed applicant is Dentsply Sirona. The 510(k) number is K234018.

When did CEREC Cercon 4D™ Abutment Blocks, CEREC Cercon 4D™ Abutment System receive FDA 510(k) clearance?

CEREC Cercon 4D™ Abutment Blocks, CEREC Cercon 4D™ Abutment System received FDA 510(k) clearance on 2024-05-07, under 510(k) number K234018.

Who is the listed applicant for CEREC Cercon 4D™ Abutment Blocks, CEREC Cercon 4D™ Abutment System?

The FDA 510(k) record lists Dentsply Sirona as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CEREC Cercon 4D™ Abutment Blocks, CEREC Cercon 4D™ Abutment System?

The FDA product code for CEREC Cercon 4D™ Abutment Blocks, CEREC Cercon 4D™ Abutment System is NHA.

Other records listing Dentsply Sirona as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260785DS Core CBCT AnatomyK260722SureSmile Aligner (ASSY500020)K253565SureSmile SoftwareK251614Stainless Steel Surgical KitsK253959Primevision 3DK253009DS Core Detect

View all 86 devices →

Related Devices (Code: NHA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare ABK261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, Inc.K253922Neodent Scannable Healing AbutmentJJGC Indústria e Comércio de Materiais Dentários S.A.K254145Omni-Directional Multi-Unit Abutment System (Trade Name: Omnibut™)Smart Denture Conversions, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑