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)

Preat Abutments

K-Number: K220823 · 2022-10-26

ApplicantPreat Corporation
Decision Date2022-10-26
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Preat Abutments is the device name listed in this FDA 510(k) record. The listed applicant is Preat Corporation. It received FDA 510(k) clearance on 2022-10-26 under 510(k) number K220823. 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 Preat Abutments?

Preat Abutments is a medical device that received FDA 510(k) clearance on 2022-10-26. The listed applicant is Preat Corporation. The 510(k) number is K220823.

When did Preat Abutments receive FDA 510(k) clearance?

Preat Abutments received FDA 510(k) clearance on 2022-10-26, under 510(k) number K220823.

Who is the listed applicant for Preat Abutments?

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

What is the FDA product code for Preat Abutments?

The FDA product code for Preat Abutments is NHA.

Other records listing Preat Corporation 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.

K243824Preat AbutmentsK183518Preat Abutments

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.

↑