Oneday Implant Abutment
K-Number: K231753 · 2024-02-21
Device Summary
Frequently Asked Questions
What is the Oneday Implant Abutment?
Oneday Implant Abutment is a medical device that received FDA 510(k) clearance on 2024-02-21. The listed applicant is Oneday Biotech Co., Ltd.. The 510(k) number is K231753.
When did Oneday Implant Abutment receive FDA 510(k) clearance?
Oneday Implant Abutment received FDA 510(k) clearance on 2024-02-21, under 510(k) number K231753.
Who is the listed applicant for Oneday Implant Abutment?
The FDA 510(k) record lists Oneday Biotech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Oneday Implant Abutment?
The FDA product code for Oneday Implant Abutment is NHA.
Other records listing Oneday Biotech 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.