FDA 510(k)

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

K-Number: K234018 · 2024-05-07

Decision Date2024-05-07

Product CodeNHA

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

CEREC Cercon 4D Abutment Blocks, CEREC Cercon 4D Abutment System is a medical device manufactured by Dentsply Sirona. It received FDA 510(k) clearance on 2024-05-07 under approval 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. It is manufactured by Dentsply Sirona. The 510(k) number is K234018.

When was CEREC Cercon 4D Abutment Blocks, CEREC Cercon 4D Abutment System approved by the FDA?

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

What company makes CEREC Cercon 4D Abutment Blocks, CEREC Cercon 4D Abutment System?

CEREC Cercon 4D Abutment Blocks, CEREC Cercon 4D Abutment System is manufactured by Dentsply Sirona.

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.

Related Clinical Trials

NCT05883202 Effect of the Abutment-Prosthesis Connection on Marginal Bone Loss and Gingival Sealing Around Dental Implants SUSPENDED NCT05951491 Improving Arm Function Using Wearable Exoskeletons SUSPENDED NCT07497451 Enhancing Pain Management Among Patients Diagnosed With Stage III and Stage IV of Breast Cancer: The Power of Immersive and Non-Immersive Virtual Reality-Driven Interactive Guided Imagery NOT_YET_RECRUITING

Other Devices by Dentsply Sirona

K161330Pour Acrylic K160825MIDWEST RDH Freedom Cordless Prophy System with SmartMode Technology K162107TPH Spectra+ Universal Composite Restorative K160626ATLANTIS Abutment for HIOSSEN ET implant K161030ATLANTIS Abutment for CONELOG implant K161269CELTRA Press

View all 65 devices →

Related Devices (Code: NHA)

K161713Dentium CAD/CAM AbutmentsDentium Co., Ltd. K160798IPS e.max® Press Abutment Solutions for Viteo Base TiIvoclar Vivadent, AG K162004PREMIUM Implant Systems SHELTA Implant SystemsSweden & Martina S.P.A. K153015Transfer & Angled AbutmentOsstem Implant Co., Ltd. K161435Temporary Snap AbutmentNobel Biocare AB K160786RODO Abutment SystemRodo Medical, Inc.

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.