EK MULTI ANGLED 30 ABUTMENT
K-Number: K251427 · 2026-01-29
ApplicantHiossen, Inc.
Decision Date2026-01-29
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
EK MULTI ANGLED 30 ABUTMENT is a medical device manufactured by Hiossen, Inc.. It received FDA 510(k) clearance on 2026-01-29 under approval number K251427. 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 EK MULTI ANGLED 30 ABUTMENT?
EK MULTI ANGLED 30 ABUTMENT is a medical device that received FDA 510(k) clearance on 2026-01-29. It is manufactured by Hiossen, Inc.. The 510(k) number is K251427.
When was EK MULTI ANGLED 30 ABUTMENT approved by the FDA?
EK MULTI ANGLED 30 ABUTMENT received FDA 510(k) clearance on 2026-01-29, under approval number K251427.
What company makes EK MULTI ANGLED 30 ABUTMENT?
EK MULTI ANGLED 30 ABUTMENT is manufactured by Hiossen, Inc..
What is the FDA product code for EK MULTI ANGLED 30 ABUTMENT?
The FDA product code for EK MULTI ANGLED 30 ABUTMENT is NHA.
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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.