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FDA 510(k)

DENTAL SCREW POSTS

K-Number: K931396 · 1994-04-28

ApplicantHarald Nordin S.A
Decision Date1994-04-28
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL SCREW POSTS 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 1994-04-28 under 510(k) number K931396. 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 DENTAL SCREW POSTS?

DENTAL SCREW POSTS is a medical device that received FDA 510(k) clearance on 1994-04-28. The listed applicant is Harald Nordin S.A. The 510(k) number is K931396.

When did DENTAL SCREW POSTS receive FDA 510(k) clearance?

DENTAL SCREW POSTS received FDA 510(k) clearance on 1994-04-28, under 510(k) number K931396.

Who is the listed applicant for DENTAL SCREW POSTS?

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 DENTAL SCREW POSTS?

The FDA product code for DENTAL SCREW POSTS is ELR.

Related Clinical Trials

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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.

K003221HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POSTK003219HARALD NORDIN CARBONITE CARBON FIBER COMPOSITE DENTAL POST

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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