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)

MISTRAL - ONE STAGE SCREW-TYPE DENTAL IMPLANT, MODEL MF9

K-Number: K070022 · 2007-04-20

ApplicantMis Implants Technologies , Ltd.
Decision Date2007-04-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MISTRAL - ONE STAGE SCREW-TYPE DENTAL IMPLANT, MODEL MF9 is the device name listed in this FDA 510(k) record. The listed applicant is Mis Implants Technologies , Ltd.. It received FDA 510(k) clearance on 2007-04-20 under 510(k) number K070022. 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 MISTRAL - ONE STAGE SCREW-TYPE DENTAL IMPLANT, MODEL MF9?

MISTRAL - ONE STAGE SCREW-TYPE DENTAL IMPLANT, MODEL MF9 is a medical device that received FDA 510(k) clearance on 2007-04-20. The listed applicant is Mis Implants Technologies , Ltd.. The 510(k) number is K070022.

When did MISTRAL - ONE STAGE SCREW-TYPE DENTAL IMPLANT, MODEL MF9 receive FDA 510(k) clearance?

MISTRAL - ONE STAGE SCREW-TYPE DENTAL IMPLANT, MODEL MF9 received FDA 510(k) clearance on 2007-04-20, under 510(k) number K070022.

Who is the listed applicant for MISTRAL - ONE STAGE SCREW-TYPE DENTAL IMPLANT, MODEL MF9?

The FDA 510(k) record lists Mis Implants Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MISTRAL - ONE STAGE SCREW-TYPE DENTAL IMPLANT, MODEL MF9?

The FDA product code for MISTRAL - ONE STAGE SCREW-TYPE DENTAL IMPLANT, MODEL MF9 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 Mis Implants Technologies , Ltd. 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.

K182228MIS LOCKiT Abutments System, OT-Equators and Ball AttachmentsK180282MIS Internal Hex Dental Implant SystemK173326MIS CONNECT Conical Connection AbutmentK172505MIS C1 Narrow Platform Conical Connection Implant System, MIS C1 Wide Platform Conical Connection AbutmentsK163349MIS V3 Conical Connection Dental Implant System­K112162CONICAL CONNECTION IMPLANTS

View all 13 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.

↑