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FDA 510(k)

ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT

K-Number: K102241 · 2011-03-23

ApplicantAnthogyr Sas
Decision Date2011-03-23
Product CodeEBW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Anthogyr Sas. It received FDA 510(k) clearance on 2011-03-23 under 510(k) number K102241. The device is classified under product code EBW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT?

ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT is a medical device that received FDA 510(k) clearance on 2011-03-23. The listed applicant is Anthogyr Sas. The 510(k) number is K102241.

When did ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT receive FDA 510(k) clearance?

ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT received FDA 510(k) clearance on 2011-03-23, under 510(k) number K102241.

Who is the listed applicant for ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT?

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

What is the FDA product code for ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT?

The FDA product code for ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT is EBW.

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 Anthogyr Sas 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: EBW)

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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