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FDA 510(k)

FIBER-METAL POST

K-Number: K060075 · 2006-03-30

ApplicantForemost Dental, LLC
Decision Date2006-03-30
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIBER-METAL POST is the device name listed in this FDA 510(k) record. The listed applicant is Foremost Dental, LLC. It received FDA 510(k) clearance on 2006-03-30 under 510(k) number K060075. 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 FIBER-METAL POST?

FIBER-METAL POST is a medical device that received FDA 510(k) clearance on 2006-03-30. The listed applicant is Foremost Dental, LLC. The 510(k) number is K060075.

When did FIBER-METAL POST receive FDA 510(k) clearance?

FIBER-METAL POST received FDA 510(k) clearance on 2006-03-30, under 510(k) number K060075.

Who is the listed applicant for FIBER-METAL POST?

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

What is the FDA product code for FIBER-METAL POST?

The FDA product code for FIBER-METAL POST is ELR.

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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.

K042848FRC POSTEC PLUSIvoclar Vivadent, Inc.K030820EVERSTICK POSTStick Tech , Ltd.K020431FIBIOCOREEst. AnthogyrK012496CARBON POSTJ. Morita USA, Inc.K013802FRC POSTECIvoclar Vivadent, Inc.K012849GLASS POSTJ. Morita USA, 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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