Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4

K-Number: K010132 · 2002-06-04

ApplicantSOADCO, S.L.
Decision Date2002-06-04
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4 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 2002-06-04 under 510(k) number K010132. 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 IMPLANTS, MODELS SK, NK, IK, S3, AND S4?

KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4 is a medical device that received FDA 510(k) clearance on 2002-06-04. The listed applicant is SOADCO, S.L.. The 510(k) number is K010132.

When did KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4 receive FDA 510(k) clearance?

KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4 received FDA 510(k) clearance on 2002-06-04, under 510(k) number K010132.

Who is the listed applicant for KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4?

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 IMPLANTS, MODELS SK, NK, IK, S3, AND S4?

The FDA product code for KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K243128Klockner KitsK230103Klockner AbutmentsK173642KLOCKNER SURGICAL BOXK170022Klockner Vega TiBase for CERECK153098KLOCKNER VEGA DENTAL IMPLANT SYSTEMK151194KLOCKNER DENTAL IMPLANT ABUTMENTS (II)

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, 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.

↑