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)

SICtapered & SICvantage tapered

K-Number: K210489 · 2022-03-17

ApplicantSic Invent AG
Decision Date2022-03-17
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SICtapered & SICvantage tapered is the device name listed in this FDA 510(k) record. The listed applicant is Sic Invent AG. It received FDA 510(k) clearance on 2022-03-17 under 510(k) number K210489. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SICtapered & SICvantage tapered?

SICtapered & SICvantage tapered is a medical device that received FDA 510(k) clearance on 2022-03-17. The listed applicant is Sic Invent AG. The 510(k) number is K210489.

When did SICtapered & SICvantage tapered receive FDA 510(k) clearance?

SICtapered & SICvantage tapered received FDA 510(k) clearance on 2022-03-17, under 510(k) number K210489.

Who is the listed applicant for SICtapered & SICvantage tapered?

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

What is the FDA product code for SICtapered & SICvantage tapered?

The FDA product code for SICtapered & SICvantage tapered is DZE.

Other records listing Sic Invent 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.

K252904SIC Abutments including CAD/CAM SolutionsK173207SIC invent Dental Implant Systems

Related Devices (Code: DZE)

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.

K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.K252731Promimic ZrP Surface Dental Implant; Promimic ZrP + HAnano Surface Dental ImplantPromimic ABK252031Adin Long Dental Implant SystemAdin Dental Implant Systems , Ltd.

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.

↑