PRE-MILLED Abutment
K-Number: K202269 · 2020-11-25
Device Summary
Frequently Asked Questions
What is the PRE-MILLED Abutment?
PRE-MILLED Abutment is a medical device that received FDA 510(k) clearance on 2020-11-25. The listed applicant is Mit Global Co., Ltd.. The 510(k) number is K202269.
When did PRE-MILLED Abutment receive FDA 510(k) clearance?
PRE-MILLED Abutment received FDA 510(k) clearance on 2020-11-25, under 510(k) number K202269.
Who is the listed applicant for PRE-MILLED Abutment?
The FDA 510(k) record lists Mit Global Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRE-MILLED Abutment?
The FDA product code for PRE-MILLED Abutment is NHA.
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.