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FDA 510(k)

EASYPROPHY SERIES AIR POLISH DEVICES, MODELS EASYPROPHY 200 AND EASYPROPHY 400

K-Number: K112869 · 2011-12-16

Decision Date2011-12-16
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

EASYPROPHY SERIES AIR POLISH DEVICES, MODELS EASYPROPHY 200 AND EASYPROPHY 400 is the device name listed in this FDA 510(k) record. The listed applicant is Beyes Dental Canada, Inc.. It received FDA 510(k) clearance on 2011-12-16 under 510(k) number K112869. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EASYPROPHY SERIES AIR POLISH DEVICES, MODELS EASYPROPHY 200 AND EASYPROPHY 400?

EASYPROPHY SERIES AIR POLISH DEVICES, MODELS EASYPROPHY 200 AND EASYPROPHY 400 is a medical device that received FDA 510(k) clearance on 2011-12-16. The listed applicant is Beyes Dental Canada, Inc.. The 510(k) number is K112869.

When did EASYPROPHY SERIES AIR POLISH DEVICES, MODELS EASYPROPHY 200 AND EASYPROPHY 400 receive FDA 510(k) clearance?

EASYPROPHY SERIES AIR POLISH DEVICES, MODELS EASYPROPHY 200 AND EASYPROPHY 400 received FDA 510(k) clearance on 2011-12-16, under 510(k) number K112869.

Who is the listed applicant for EASYPROPHY SERIES AIR POLISH DEVICES, MODELS EASYPROPHY 200 AND EASYPROPHY 400?

The FDA 510(k) record lists Beyes Dental Canada, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EASYPROPHY SERIES AIR POLISH DEVICES, MODELS EASYPROPHY 200 AND EASYPROPHY 400?

The FDA product code for EASYPROPHY SERIES AIR POLISH DEVICES, MODELS EASYPROPHY 200 AND EASYPROPHY 400 is EFB.

Related Clinical Trials

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.

Other records listing Beyes Dental Canada, Inc. 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: EFB)

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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