FDA 510(k)

VOCO Retraction Paste

K-Number: K213149 · 2021-12-09

Decision Date2021-12-09

Product CodeMVL

DecisionSubstantially Equivalent

Device Summary

VOCO Retraction Paste is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2021-12-09 under 510(k) number K213149. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VOCO Retraction Paste?

VOCO Retraction Paste is a medical device that received FDA 510(k) clearance on 2021-12-09. The listed applicant is Voco GmbH. The 510(k) number is K213149.

When did VOCO Retraction Paste receive FDA 510(k) clearance?

VOCO Retraction Paste received FDA 510(k) clearance on 2021-12-09, under 510(k) number K213149.

Who is the listed applicant for VOCO Retraction Paste?

The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VOCO Retraction Paste?

The FDA product code for VOCO Retraction Paste is MVL.

Other records listing Voco GmbH 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.

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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.