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FDA 510(k)

Klockner Vega TiBase for CEREC

K-Number: K170022 · 2017-11-16

ApplicantSOADCO, S.L.
Decision Date2017-11-16
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Klockner Vega TiBase for CEREC 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 2017-11-16 under 510(k) number K170022. 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 Vega TiBase for CEREC?

Klockner Vega TiBase for CEREC is a medical device that received FDA 510(k) clearance on 2017-11-16. The listed applicant is SOADCO, S.L.. The 510(k) number is K170022.

When did Klockner Vega TiBase for CEREC receive FDA 510(k) clearance?

Klockner Vega TiBase for CEREC received FDA 510(k) clearance on 2017-11-16, under 510(k) number K170022.

Who is the listed applicant for Klockner Vega TiBase for CEREC?

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 Vega TiBase for CEREC?

The FDA product code for Klockner Vega TiBase for CEREC is NHA.

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 BOXK153098KLOCKNER VEGA DENTAL IMPLANT SYSTEMK151194KLOCKNER DENTAL IMPLANT ABUTMENTS (II)

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

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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