CreoDent Solidex Customized Abutment and Screw
K-Number: K220390 · 2022-12-02
ApplicantCreodent Prosthetics, Ltd.
Decision Date2022-12-02
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
CreoDent Solidex Customized Abutment and Screw is a medical device manufactured by Creodent Prosthetics, Ltd.. It received FDA 510(k) clearance on 2022-12-02 under approval number K220390. 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 CreoDent Solidex Customized Abutment and Screw?
CreoDent Solidex Customized Abutment and Screw is a medical device that received FDA 510(k) clearance on 2022-12-02. It is manufactured by Creodent Prosthetics, Ltd.. The 510(k) number is K220390.
When was CreoDent Solidex Customized Abutment and Screw approved by the FDA?
CreoDent Solidex Customized Abutment and Screw received FDA 510(k) clearance on 2022-12-02, under approval number K220390.
What company makes CreoDent Solidex Customized Abutment and Screw?
CreoDent Solidex Customized Abutment and Screw is manufactured by Creodent Prosthetics, Ltd..
What is the FDA product code for CreoDent Solidex Customized Abutment and Screw?
The FDA product code for CreoDent Solidex Customized Abutment and Screw is NHA.
Related Clinical Trials
Other Devices by Creodent Prosthetics, Ltd.
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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.