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FDA 510(k)

BEGO SEMADOS S-LINE

K-Number: K090716 · 2009-10-06

ApplicantBego Implant Systems GmbH & Co. KG
Decision Date2009-10-06
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BEGO SEMADOS S-LINE is the device name listed in this FDA 510(k) record. The listed applicant is Bego Implant Systems GmbH & Co. KG. It received FDA 510(k) clearance on 2009-10-06 under 510(k) number K090716. 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 BEGO SEMADOS S-LINE?

BEGO SEMADOS S-LINE is a medical device that received FDA 510(k) clearance on 2009-10-06. The listed applicant is Bego Implant Systems GmbH & Co. KG. The 510(k) number is K090716.

When did BEGO SEMADOS S-LINE receive FDA 510(k) clearance?

BEGO SEMADOS S-LINE received FDA 510(k) clearance on 2009-10-06, under 510(k) number K090716.

Who is the listed applicant for BEGO SEMADOS S-LINE?

The FDA 510(k) record lists Bego Implant Systems GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BEGO SEMADOS S-LINE?

The FDA product code for BEGO SEMADOS S-LINE 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 Bego Implant Systems GmbH & Co. KG 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.

K201412BEGO SEMADOS Tr 58350; BEGO SEMADOS RS/RSX-Line Tray Plus, BEGO Semados Tr 58349; BEGO Semados Tr 58348, BEGO Semados DSTr 58356; Drill Stop Tray Plus (RS/RSX-Line), BEGO SEMADOS PKTr 58357; Prosthetic KitK201700BEGO Semados® RS/RSX Implant System

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.

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