Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MONTBLANC SURGICAL CONTRA-ANGLE AND STRAIGHT HANDPIECE

K-Number: K111532 · 2011-10-07

ApplicantAnthogyr Sas
Decision Date2011-10-07
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MONTBLANC SURGICAL CONTRA-ANGLE AND STRAIGHT HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Anthogyr Sas. It received FDA 510(k) clearance on 2011-10-07 under 510(k) number K111532. 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 MONTBLANC SURGICAL CONTRA-ANGLE AND STRAIGHT HANDPIECE?

MONTBLANC SURGICAL CONTRA-ANGLE AND STRAIGHT HANDPIECE is a medical device that received FDA 510(k) clearance on 2011-10-07. The listed applicant is Anthogyr Sas. The 510(k) number is K111532.

When did MONTBLANC SURGICAL CONTRA-ANGLE AND STRAIGHT HANDPIECE receive FDA 510(k) clearance?

MONTBLANC SURGICAL CONTRA-ANGLE AND STRAIGHT HANDPIECE received FDA 510(k) clearance on 2011-10-07, under 510(k) number K111532.

Who is the listed applicant for MONTBLANC SURGICAL CONTRA-ANGLE AND STRAIGHT HANDPIECE?

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 MONTBLANC SURGICAL CONTRA-ANGLE AND STRAIGHT HANDPIECE?

The FDA product code for MONTBLANC SURGICAL CONTRA-ANGLE AND STRAIGHT HANDPIECE 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 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.

K161177Axiom PXK102241ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNITK101913ANTHOFIT OI, ANTHOFIT HE, OSSFIT AND AXIOM

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.K220346Lotus Prophy AngleAjk Engineering, Inc.

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.

↑