s-Clean Link Abutment Narrow
K-Number: K230523 · 2023-05-24
Device Summary
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. The listed applicant is Dentis Co., Ltd.. The 510(k) number is K230523.
When did s-Clean Link Abutment Narrow receive FDA 510(k) clearance?
s-Clean Link Abutment Narrow received FDA 510(k) clearance on 2023-05-24, under 510(k) number K230523.
Who is the listed applicant for s-Clean Link Abutment Narrow?
The FDA 510(k) record lists Dentis Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for s-Clean Link Abutment Narrow?
The FDA product code for s-Clean Link Abutment Narrow is NHA.
Other records listing Dentis Co., Ltd. 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.
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.
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.