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FDA 510(k)

ANTHOGYR CONTRA ANGLES AND HANDPIECES

K-Number: K060317 · 2006-04-28

ApplicantEst. Anthogyr
Decision Date2006-04-28
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ANTHOGYR CONTRA ANGLES AND HANDPIECES is the device name listed in this FDA 510(k) record. The listed applicant is Est. Anthogyr. It received FDA 510(k) clearance on 2006-04-28 under 510(k) number K060317. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANTHOGYR CONTRA ANGLES AND HANDPIECES?

ANTHOGYR CONTRA ANGLES AND HANDPIECES is a medical device that received FDA 510(k) clearance on 2006-04-28. The listed applicant is Est. Anthogyr. The 510(k) number is K060317.

When did ANTHOGYR CONTRA ANGLES AND HANDPIECES receive FDA 510(k) clearance?

ANTHOGYR CONTRA ANGLES AND HANDPIECES received FDA 510(k) clearance on 2006-04-28, under 510(k) number K060317.

Who is the listed applicant for ANTHOGYR CONTRA ANGLES AND HANDPIECES?

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

What is the FDA product code for ANTHOGYR CONTRA ANGLES AND HANDPIECES?

The FDA product code for ANTHOGYR CONTRA ANGLES AND HANDPIECES is EGS.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Est. Anthogyr 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.

K070084MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROLK020431FIBIOCORE

Related Devices (Code: EGS)

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.

K251869Disposable Prophy Angle (3399-60, 3399-090, 3399-105)Premium Plus (Dongguan) LimitedK240950Disposable Prophy AnglePacific Care LimitedK240183Star E900 Handpiece SeriesDentalez, Inc., Stardental DivisionK230106General Cutting StraightNakanishi, Inc.K222518FX ContraNakanishi, Inc.K220874Smooth Drive contra angle and straight handpiecesLares Research

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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