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FDA 510(k)

Oneday Implant Abutment

K-Number: K231753 · 2024-02-21

ApplicantOneday Biotech Co., Ltd.
Decision Date2024-02-21
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Oneday Implant Abutment is a medical device manufactured by Oneday Biotech Co., Ltd.. It received FDA 510(k) clearance on 2024-02-21 under approval number K231753. 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 Oneday Implant Abutment?

Oneday Implant Abutment is a medical device that received FDA 510(k) clearance on 2024-02-21. It is manufactured by Oneday Biotech Co., Ltd.. The 510(k) number is K231753.

When was Oneday Implant Abutment approved by the FDA?

Oneday Implant Abutment received FDA 510(k) clearance on 2024-02-21, under approval number K231753.

What company makes Oneday Implant Abutment?

Oneday Implant Abutment is manufactured by Oneday Biotech Co., Ltd..

What is the FDA product code for Oneday Implant Abutment?

The FDA product code for Oneday Implant Abutment is NHA.

Related Clinical Trials

NCT07246499 Multicentre Study on the Impact of Transmucosal Abutment Surface Characteristics on Peri-implant Tissues. ACTIVE_NOT_RECRUITING NCT05883202 Effect of the Abutment-Prosthesis Connection on Marginal Bone Loss and Gingival Sealing Around Dental Implants SUSPENDED NCT06636136 Transtibial Osseointegration RECRUITING

Other Devices by Oneday Biotech Co., Ltd.

K222946Oneday Mini Implant System

Related Devices (Code: 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.

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