n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks,
K-Number: K160262 · 2016-09-16
Device Summary
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. The listed applicant is Institut Straumann AG. The 510(k) number is K160262.
When did n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks, receive FDA 510(k) clearance?
n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks, received FDA 510(k) clearance on 2016-09-16, under 510(k) number K160262.
Who is the listed applicant for n!ce LT Glass Ceramic Blocks, n!ce HT Glass Ceramic Blocks,?
The FDA 510(k) record lists Institut Straumann AG as the applicant. This does not by itself establish the device manufacturer.
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.
Other records listing Institut Straumann AG as applicant
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.
Related Devices (Code: EIH)
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.