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FDA 510(k)

DGA Abutment

K-Number: K231210 · 2024-03-05

ApplicantModern Dental Laboratory (Dg) Co., Ltd.
Decision Date2024-03-05
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DGA Abutment is a medical device manufactured by Modern Dental Laboratory (Dg) Co., Ltd.. It received FDA 510(k) clearance on 2024-03-05 under approval 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. It is manufactured by Modern Dental Laboratory (Dg) Co., Ltd.. The 510(k) number is K231210.

When was DGA Abutment approved by the FDA?

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

What company makes DGA Abutment?

DGA Abutment is manufactured by Modern Dental Laboratory (Dg) Co., Ltd..

What is the FDA product code for DGA Abutment?

The FDA product code for DGA Abutment is NHA.

Other Devices by Modern Dental Laboratory (Dg) Co., Ltd.

K231884TRIOCLEAR System

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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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