ET Hybrid Abutment
K-Number: K162390 · 2017-01-30
ApplicantHiossen, Inc.
Decision Date2017-01-30
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
ET Hybrid Abutment is a medical device manufactured by Hiossen, Inc.. It received FDA 510(k) clearance on 2017-01-30 under approval number K162390. 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 ET Hybrid Abutment?
ET Hybrid Abutment is a medical device that received FDA 510(k) clearance on 2017-01-30. It is manufactured by Hiossen, Inc.. The 510(k) number is K162390.
When was ET Hybrid Abutment approved by the FDA?
ET Hybrid Abutment received FDA 510(k) clearance on 2017-01-30, under approval number K162390.
What company makes ET Hybrid Abutment?
ET Hybrid Abutment is manufactured by Hiossen, Inc..
What is the FDA product code for ET Hybrid Abutment?
The FDA product code for ET Hybrid Abutment is NHA.
Other Devices by Hiossen, 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.