Dentis s-Clean Abutment Mini
K-Number: K220440 · 2022-06-16
Device Summary
Frequently Asked Questions
What is the Dentis s-Clean Abutment Mini?
Dentis s-Clean Abutment Mini is a medical device that received FDA 510(k) clearance on 2022-06-16. The listed applicant is Dentis Co., Ltd.. The 510(k) number is K220440.
When did Dentis s-Clean Abutment Mini receive FDA 510(k) clearance?
Dentis s-Clean Abutment Mini received FDA 510(k) clearance on 2022-06-16, under 510(k) number K220440.
Who is the listed applicant for Dentis s-Clean Abutment Mini?
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 Dentis s-Clean Abutment Mini?
The FDA product code for Dentis s-Clean Abutment Mini 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.