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FDA 510(k)

ZENO AI ECO DISC

K-Number: K082257 · 2008-09-18

Decision Date2008-09-18
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZENO AI ECO DISC is the device name listed in this FDA 510(k) record. The listed applicant is Wieland Dental + Technik GmbH & Co. KG. It received FDA 510(k) clearance on 2008-09-18 under 510(k) number K082257. 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 ZENO AI ECO DISC?

ZENO AI ECO DISC is a medical device that received FDA 510(k) clearance on 2008-09-18. The listed applicant is Wieland Dental + Technik GmbH & Co. KG. The 510(k) number is K082257.

When did ZENO AI ECO DISC receive FDA 510(k) clearance?

ZENO AI ECO DISC received FDA 510(k) clearance on 2008-09-18, under 510(k) number K082257.

Who is the listed applicant for ZENO AI ECO 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 AI ECO DISC?

The FDA product code for ZENO AI ECO 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.

View all 42 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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