n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks,
K-Number: K160262 · 2016-09-16
ApplicantInstitut Straumann AG
Decision Date2016-09-16
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks, is a medical device manufactured by Institut Straumann AG. It received FDA 510(k) clearance on 2016-09-16 under approval number K160262. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks,?
n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks, is a medical device that received FDA 510(k) clearance on 2016-09-16. It is manufactured by Institut Straumann AG. The 510(k) number is K160262.
When was n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks, approved by the FDA?
n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks, received FDA 510(k) clearance on 2016-09-16, under approval number K160262.
What company makes n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks,?
n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks, is manufactured by Institut Straumann AG.
What is the FDA product code for n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks,?
The FDA product code for n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks, is EIH.
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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.