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FDA 510(k)

Meta G UCLA Abutment

K-Number: K232546 · 2023-11-21

Decision Date2023-11-21
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Meta G UCLA Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Cowellmedi Co., Ltd.. It received FDA 510(k) clearance on 2023-11-21 under 510(k) number K232546. 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 Meta G UCLA Abutment?

Meta G UCLA Abutment is a medical device that received FDA 510(k) clearance on 2023-11-21. The listed applicant is Cowellmedi Co., Ltd.. The 510(k) number is K232546.

When did Meta G UCLA Abutment receive FDA 510(k) clearance?

Meta G UCLA Abutment received FDA 510(k) clearance on 2023-11-21, under 510(k) number K232546.

Who is the listed applicant for Meta G UCLA Abutment?

The FDA 510(k) record lists Cowellmedi Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Meta G UCLA Abutment?

The FDA product code for Meta G UCLA Abutment is NHA.

Other records listing Cowellmedi 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.

View all 7 devices →

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.