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FDA 510(k)

KLOCKNER DENTAL IMPLANT, MODEL S3M

K-Number: K052654 · 2006-01-30

ApplicantSOADCO, S.L.
Decision Date2006-01-30
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KLOCKNER DENTAL IMPLANT, MODEL S3M is the device name listed in this FDA 510(k) record. The listed applicant is SOADCO, S.L.. It received FDA 510(k) clearance on 2006-01-30 under 510(k) number K052654. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KLOCKNER DENTAL IMPLANT, MODEL S3M?

KLOCKNER DENTAL IMPLANT, MODEL S3M is a medical device that received FDA 510(k) clearance on 2006-01-30. The listed applicant is SOADCO, S.L.. The 510(k) number is K052654.

When did KLOCKNER DENTAL IMPLANT, MODEL S3M receive FDA 510(k) clearance?

KLOCKNER DENTAL IMPLANT, MODEL S3M received FDA 510(k) clearance on 2006-01-30, under 510(k) number K052654.

Who is the listed applicant for KLOCKNER DENTAL IMPLANT, MODEL S3M?

The FDA 510(k) record lists SOADCO, S.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KLOCKNER DENTAL IMPLANT, MODEL S3M?

The FDA product code for KLOCKNER DENTAL IMPLANT, MODEL S3M is DZE.

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 SOADCO, S.L. 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.

View all 11 devices →

Related Devices (Code: DZE)

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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