s-Clean Link Abutment Narrow
K-Number: K230523 · 2023-05-24
ApplicantDentis Co., Ltd.
Decision Date2023-05-24
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
s-Clean Link Abutment Narrow is a medical device manufactured by Dentis Co., Ltd.. It received FDA 510(k) clearance on 2023-05-24 under approval number K230523. 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 s-Clean Link Abutment Narrow?
s-Clean Link Abutment Narrow is a medical device that received FDA 510(k) clearance on 2023-05-24. It is manufactured by Dentis Co., Ltd.. The 510(k) number is K230523.
When was s-Clean Link Abutment Narrow approved by the FDA?
s-Clean Link Abutment Narrow received FDA 510(k) clearance on 2023-05-24, under approval number K230523.
What company makes s-Clean Link Abutment Narrow?
s-Clean Link Abutment Narrow is manufactured by Dentis Co., Ltd..
What is the FDA product code for s-Clean Link Abutment Narrow?
The FDA product code for s-Clean Link Abutment Narrow is NHA.
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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.