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FDA 510(k)

NobelProcera Zirconia N1 Base

K-Number: K220048 · 2022-07-29

ApplicantNobel Biocare Services AG
Decision Date2022-07-29
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NobelProcera Zirconia N1 Base is the device name listed in this FDA 510(k) record. The listed applicant is Nobel Biocare Services AG. It received FDA 510(k) clearance on 2022-07-29 under 510(k) number K220048. 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 NobelProcera Zirconia N1 Base?

NobelProcera Zirconia N1 Base is a medical device that received FDA 510(k) clearance on 2022-07-29. The listed applicant is Nobel Biocare Services AG. The 510(k) number is K220048.

When did NobelProcera Zirconia N1 Base receive FDA 510(k) clearance?

NobelProcera Zirconia N1 Base received FDA 510(k) clearance on 2022-07-29, under 510(k) number K220048.

Who is the listed applicant for NobelProcera Zirconia N1 Base?

The FDA 510(k) record lists Nobel Biocare Services AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NobelProcera Zirconia N1 Base?

The FDA product code for NobelProcera Zirconia N1 Base is NHA.

Other records listing Nobel Biocare Services AG 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.

K231219NobelZygoma PureSet™ TrayK220339Esthetic Abutments Nobel Biocare N1K211109N1 TiUltra TCC Implant SystemK212932Nobel Biocare NobelSpeedy Groovy / Branemark System Mk III TiUnite / Replace Select TC PureSet Tray

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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