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FDA 510(k)

KLOCKNER DENTAL IMPLANT ABUTMENTS (II)

K-Number: K151194 · 2016-01-29

ApplicantSOADCO, S.L.
Decision Date2016-01-29
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KLOCKNER DENTAL IMPLANT ABUTMENTS (II) is the device name listed in this FDA 510(k) record. The listed applicant is SOADCO, S.L.. It received FDA 510(k) clearance on 2016-01-29 under 510(k) number K151194. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KLOCKNER DENTAL IMPLANT ABUTMENTS (II)?

KLOCKNER DENTAL IMPLANT ABUTMENTS (II) is a medical device that received FDA 510(k) clearance on 2016-01-29. The listed applicant is SOADCO, S.L.. The 510(k) number is K151194.

When did KLOCKNER DENTAL IMPLANT ABUTMENTS (II) receive FDA 510(k) clearance?

KLOCKNER DENTAL IMPLANT ABUTMENTS (II) received FDA 510(k) clearance on 2016-01-29, under 510(k) number K151194.

Who is the listed applicant for KLOCKNER DENTAL IMPLANT ABUTMENTS (II)?

The FDA 510(k) record lists SOADCO, S.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KLOCKNER DENTAL IMPLANT ABUTMENTS (II)?

The FDA product code for KLOCKNER DENTAL IMPLANT ABUTMENTS (II) is NHA.

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.

NCT05122897Investigation of Biofilm Formation on Temporary push-on Rings of Implant CrownsRECRUITINGNCT05883202Effect of the Abutment-Prosthesis Connection on Marginal Bone Loss and Gingival Sealing Around Dental ImplantsSUSPENDEDNCT07246499Multicentre Study on the Impact of Transmucosal Abutment Surface Characteristics on Peri-implant Tissues.COMPLETEDNCT07714265Soft Tissue Augmentation Around Dental Implants Using Connective Tissue Graft, Submerged Tenting Abutment, or Sub-crestal Implant PlacementRECRUITING

Other records listing SOADCO, S.L. 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.

K243128Klockner KitsK230103Klockner AbutmentsK173642KLOCKNER SURGICAL BOXK170022Klockner Vega TiBase for CERECK153098KLOCKNER VEGA DENTAL IMPLANT SYSTEM

Related Devices (Code: NHA)

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.

K253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare ABK261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLCK260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, Inc.K253922Neodent Scannable Healing AbutmentJJGC Indústria e Comércio de Materiais Dentários S.A.K254145Omni-Directional Multi-Unit Abutment System (Trade Name: Omnibut™)Smart Denture Conversions, LLC

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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