Straumann Variobase Abutments XC for Bridge/Bar
K-Number: K253315 · 2026-01-22
ApplicantInstitut Straumann AG
Decision Date2026-01-22
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Straumann Variobase Abutments XC for Bridge/Bar is a medical device manufactured by Institut Straumann AG. It received FDA 510(k) clearance on 2026-01-22 under approval number K253315. 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 Straumann Variobase Abutments XC for Bridge/Bar?
Straumann Variobase Abutments XC for Bridge/Bar is a medical device that received FDA 510(k) clearance on 2026-01-22. It is manufactured by Institut Straumann AG. The 510(k) number is K253315.
When was Straumann Variobase Abutments XC for Bridge/Bar approved by the FDA?
Straumann Variobase Abutments XC for Bridge/Bar received FDA 510(k) clearance on 2026-01-22, under approval number K253315.
What company makes Straumann Variobase Abutments XC for Bridge/Bar?
Straumann Variobase Abutments XC for Bridge/Bar is manufactured by Institut Straumann AG.
What is the FDA product code for Straumann Variobase Abutments XC for Bridge/Bar?
The FDA product code for Straumann Variobase Abutments XC for Bridge/Bar 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.