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)

KIS-V PRE-ANGULATED AND WIDE BODY ABUTMENTS

K-Number: K950893 · 1995-05-05

ApplicantThe Implant Center of the Palm Beaches
Decision Date1995-05-05
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KIS-V PRE-ANGULATED AND WIDE BODY ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is The Implant Center of the Palm Beaches. It received FDA 510(k) clearance on 1995-05-05 under 510(k) number K950893. 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 KIS-V PRE-ANGULATED AND WIDE BODY ABUTMENTS?

KIS-V PRE-ANGULATED AND WIDE BODY ABUTMENTS is a medical device that received FDA 510(k) clearance on 1995-05-05. The listed applicant is The Implant Center of the Palm Beaches. The 510(k) number is K950893.

When did KIS-V PRE-ANGULATED AND WIDE BODY ABUTMENTS receive FDA 510(k) clearance?

KIS-V PRE-ANGULATED AND WIDE BODY ABUTMENTS received FDA 510(k) clearance on 1995-05-05, under 510(k) number K950893.

Who is the listed applicant for KIS-V PRE-ANGULATED AND WIDE BODY ABUTMENTS?

The FDA 510(k) record lists The Implant Center of the Palm Beaches as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KIS-V PRE-ANGULATED AND WIDE BODY ABUTMENTS?

The FDA product code for KIS-V PRE-ANGULATED AND WIDE BODY ABUTMENTS 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 The Implant Center of the Palm Beaches 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.

K974280ABUTMENT - COMPLETEK960111KIS MT4K960110KIS MT3K960112KIS MT5K955048KIS MED THREAD IMPLANT & PROSTHESIS SYSTEMK953558KIS II LG HEX SCREW & CYLINDER IMPLANTS

View all 12 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.

↑