Angled Abutment
K-Number: K232560 · 2023-12-19
Device Summary
Frequently Asked Questions
What is the Angled Abutment?
Angled Abutment is a medical device that received FDA 510(k) clearance on 2023-12-19. The listed applicant is Arum Dentistry Co., Ltd.. The 510(k) number is K232560.
When did Angled Abutment receive FDA 510(k) clearance?
Angled Abutment received FDA 510(k) clearance on 2023-12-19, under 510(k) number K232560.
Who is the listed applicant for Angled Abutment?
The FDA 510(k) record lists Arum Dentistry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Angled Abutment?
The FDA product code for Angled Abutment is NHA.
Other records listing Arum Dentistry 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.