ZENO ZR DISC
K-Number: K073108 · 2007-11-21
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Device Summary
Frequently Asked Questions
What is the ZENO ZR DISC?
ZENO ZR DISC is a medical device that received FDA 510(k) clearance on 2007-11-21. The listed applicant is Wieland Dental + Technik GmbH & Co. KG. The 510(k) number is K073108.
When did ZENO ZR DISC receive FDA 510(k) clearance?
ZENO ZR DISC received FDA 510(k) clearance on 2007-11-21, under 510(k) number K073108.
Who is the listed applicant for ZENO ZR DISC?
The FDA 510(k) record lists Wieland Dental + Technik GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZENO ZR DISC?
The FDA product code for ZENO ZR DISC is EIH.
Other records listing Wieland Dental + Technik GmbH & Co. KG 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.
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