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FDA 510(k)

FRIOS ALGIPORE

K-Number: K023799 · 2003-02-05

ApplicantFriadent GmbH
Decision Date2003-02-05
Product CodeLYC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FRIOS ALGIPORE is the device name listed in this FDA 510(k) record. The listed applicant is Friadent GmbH. It received FDA 510(k) clearance on 2003-02-05 under 510(k) number K023799. The device is classified under product code LYC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRIOS ALGIPORE?

FRIOS ALGIPORE is a medical device that received FDA 510(k) clearance on 2003-02-05. The listed applicant is Friadent GmbH. The 510(k) number is K023799.

When did FRIOS ALGIPORE receive FDA 510(k) clearance?

FRIOS ALGIPORE received FDA 510(k) clearance on 2003-02-05, under 510(k) number K023799.

Who is the listed applicant for FRIOS ALGIPORE?

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

What is the FDA product code for FRIOS ALGIPORE?

The FDA product code for FRIOS ALGIPORE is LYC.

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Other records listing Friadent GmbH 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.

K040170FRIADENT PLUS DENTAL IMPLANT SYSTEMSK041509ANKYLOS DENTAL IMPLANT SYSTEMK040946ANKYLOS DENTAL IMPLANT SYSTEMK032302XIVE TG ABUTMENTSK032158XIVE DENTAL IMPLANT SYSTEM MULTIPLEK032284XIVE TG DENTAL IMPLANT SYSTEM

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Related Devices (Code: LYC)

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.

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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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