KDG Abutments
K-Number: K221381 · 2022-08-10
ApplicantKeystone Dental, Inc.
Decision Date2022-08-10
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
KDG Abutments is a medical device manufactured by Keystone Dental, Inc.. It received FDA 510(k) clearance on 2022-08-10 under approval number K221381. 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 KDG Abutments?
KDG Abutments is a medical device that received FDA 510(k) clearance on 2022-08-10. It is manufactured by Keystone Dental, Inc.. The 510(k) number is K221381.
When was KDG Abutments approved by the FDA?
KDG Abutments received FDA 510(k) clearance on 2022-08-10, under approval number K221381.
What company makes KDG Abutments?
KDG Abutments is manufactured by Keystone Dental, Inc..
What is the FDA product code for KDG Abutments?
The FDA product code for KDG Abutments is NHA.
Other Devices by Keystone Dental, Inc.
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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.