MIS Angulated multi-unit abutments
K-Number: K213432 · 2022-04-01
Device Summary
Frequently Asked Questions
What is the MIS Angulated multi-unit abutments?
MIS Angulated multi-unit abutments is a medical device that received FDA 510(k) clearance on 2022-04-01. The listed applicant is Dentsply Sirona. The 510(k) number is K213432.
When did MIS Angulated multi-unit abutments receive FDA 510(k) clearance?
MIS Angulated multi-unit abutments received FDA 510(k) clearance on 2022-04-01, under 510(k) number K213432.
Who is the listed applicant for MIS Angulated multi-unit abutments?
The FDA 510(k) record lists Dentsply Sirona as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MIS Angulated multi-unit abutments?
The FDA product code for MIS Angulated multi-unit abutments is NHA.
Other records listing Dentsply Sirona 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.