Angled Abutment
K-Number: K232560 · 2023-12-19
ApplicantArum Dentistry Co., Ltd.
Decision Date2023-12-19
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Angled Abutment is a medical device manufactured by Arum Dentistry Co., Ltd.. It received FDA 510(k) clearance on 2023-12-19 under approval number K232560. 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 Angled Abutment?
Angled Abutment is a medical device that received FDA 510(k) clearance on 2023-12-19. It is manufactured by Arum Dentistry Co., Ltd.. The 510(k) number is K232560.
When was Angled Abutment approved by the FDA?
Angled Abutment received FDA 510(k) clearance on 2023-12-19, under approval number K232560.
What company makes Angled Abutment?
Angled Abutment is manufactured by Arum Dentistry Co., Ltd..
What is the FDA product code for Angled Abutment?
The FDA product code for Angled Abutment is NHA.
Other Devices by Arum Dentistry Co., Ltd.
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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.