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FDA 510(k)

DGA Abutment

K-Number: K231210 · 2024-03-05

Decision Date2024-03-05
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DGA Abutment is the device name listed in this FDA 510(k) record. The listed applicant is Modern Dental Laboratory (Dg) Co., Ltd.. It received FDA 510(k) clearance on 2024-03-05 under 510(k) number K231210. 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 DGA Abutment?

DGA Abutment is a medical device that received FDA 510(k) clearance on 2024-03-05. The listed applicant is Modern Dental Laboratory (Dg) Co., Ltd.. The 510(k) number is K231210.

When did DGA Abutment receive FDA 510(k) clearance?

DGA Abutment received FDA 510(k) clearance on 2024-03-05, under 510(k) number K231210.

Who is the listed applicant for DGA Abutment?

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

What is the FDA product code for DGA Abutment?

The FDA product code for DGA Abutment is NHA.

Other records listing Modern Dental Laboratory (Dg) 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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.