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FDA 510(k)

ENDODONTIC PAPER POINTS

K-Number: K812886 · 1981-11-16

Decision Date1981-11-16
Product CodeEKN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDODONTIC PAPER POINTS is the device name listed in this FDA 510(k) record. The listed applicant is United Dental Mfg., Inc.. It received FDA 510(k) clearance on 1981-11-16 under 510(k) number K812886. The device is classified under product code EKN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDODONTIC PAPER POINTS?

ENDODONTIC PAPER POINTS is a medical device that received FDA 510(k) clearance on 1981-11-16. The listed applicant is United Dental Mfg., Inc.. The 510(k) number is K812886.

When did ENDODONTIC PAPER POINTS receive FDA 510(k) clearance?

ENDODONTIC PAPER POINTS received FDA 510(k) clearance on 1981-11-16, under 510(k) number K812886.

Who is the listed applicant for ENDODONTIC PAPER POINTS?

The FDA 510(k) record lists United Dental Mfg., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDODONTIC PAPER POINTS?

The FDA product code for ENDODONTIC PAPER POINTS is EKN.

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 United Dental Mfg., Inc. 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: EKN)

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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