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FDA 510(k)

ROOT CANAL POST

K-Number: K802515 · 1980-11-12

ApplicantUnitek Corp.
Decision Date1980-11-12
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ROOT CANAL POST is the device name listed in this FDA 510(k) record. The listed applicant is Unitek Corp.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802515. The device is classified under product code ELR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ROOT CANAL POST?

ROOT CANAL POST is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Unitek Corp.. The 510(k) number is K802515.

When did ROOT CANAL POST receive FDA 510(k) clearance?

ROOT CANAL POST received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802515.

Who is the listed applicant for ROOT CANAL POST?

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

What is the FDA product code for ROOT CANAL POST?

The FDA product code for ROOT CANAL POST is ELR.

Related Clinical Trials

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Other records listing Unitek Corp. 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.

K944286METAL-LINED TRANSCEND CERAMIC BRACKETK933501ALASTIKK940165ALASTIKK923999ALASTIK NSK924645TRANSCEND SERIES 6000 DEBONDING INSTRUMENTSK924295DEBRACKETING INSTRUMENT

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Related Devices (Code: ELR)

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.

K060075FIBER-METAL POSTForemost Dental, LLCK042848FRC POSTEC PLUSIvoclar Vivadent, Inc.K030820EVERSTICK POSTStick Tech , Ltd.K020431FIBIOCOREEst. AnthogyrK012496CARBON POSTJ. Morita USA, Inc.K013802FRC POSTECIvoclar Vivadent, Inc.

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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