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FDA 510(k)

CODENT DENTAL AIR-POWERED HANDPIECE, MODEL HPS

K-Number: K033213 · 2004-02-06

Decision Date2004-02-06
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CODENT DENTAL AIR-POWERED HANDPIECE, MODEL HPS is the device name listed in this FDA 510(k) record. The listed applicant is Codent Technical Industry Co., Ltd.. It received FDA 510(k) clearance on 2004-02-06 under 510(k) number K033213. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODENT DENTAL AIR-POWERED HANDPIECE, MODEL HPS?

CODENT DENTAL AIR-POWERED HANDPIECE, MODEL HPS is a medical device that received FDA 510(k) clearance on 2004-02-06. The listed applicant is Codent Technical Industry Co., Ltd.. The 510(k) number is K033213.

When did CODENT DENTAL AIR-POWERED HANDPIECE, MODEL HPS receive FDA 510(k) clearance?

CODENT DENTAL AIR-POWERED HANDPIECE, MODEL HPS received FDA 510(k) clearance on 2004-02-06, under 510(k) number K033213.

Who is the listed applicant for CODENT DENTAL AIR-POWERED HANDPIECE, MODEL HPS?

The FDA 510(k) record lists Codent Technical Industry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CODENT DENTAL AIR-POWERED HANDPIECE, MODEL HPS?

The FDA product code for CODENT DENTAL AIR-POWERED HANDPIECE, MODEL HPS is EFB.

Related Clinical Trials

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.

Other records listing Codent Technical Industry Co., Ltd. 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.

Related Devices (Code: EFB)

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.

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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