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FDA 510(k)

HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST

K-Number: K003221 · 2000-10-25

ApplicantHarald Nordin S.A
Decision Date2000-10-25
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST is the device name listed in this FDA 510(k) record. The listed applicant is Harald Nordin S.A. It received FDA 510(k) clearance on 2000-10-25 under 510(k) number K003221. 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 HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST?

HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST is a medical device that received FDA 510(k) clearance on 2000-10-25. The listed applicant is Harald Nordin S.A. The 510(k) number is K003221.

When did HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST receive FDA 510(k) clearance?

HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST received FDA 510(k) clearance on 2000-10-25, under 510(k) number K003221.

Who is the listed applicant for HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST?

The FDA 510(k) record lists Harald Nordin S.A as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST?

The FDA product code for HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST is ELR.

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Other records listing Harald Nordin S.A 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.

K003219HARALD NORDIN CARBONITE CARBON FIBER COMPOSITE DENTAL POSTK931396DENTAL SCREW POSTS

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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