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FDA 510(k)

BESTALOY

K-Number: K033434 · 2003-11-12

ApplicantWe Dong Myung Dental Industrial Co., Ltd.
Decision Date2003-11-12
Product CodeEJJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BESTALOY is the device name listed in this FDA 510(k) record. The listed applicant is We Dong Myung Dental Industrial Co., Ltd.. It received FDA 510(k) clearance on 2003-11-12 under 510(k) number K033434. The device is classified under product code EJJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BESTALOY?

BESTALOY is a medical device that received FDA 510(k) clearance on 2003-11-12. The listed applicant is We Dong Myung Dental Industrial Co., Ltd.. The 510(k) number is K033434.

When did BESTALOY receive FDA 510(k) clearance?

BESTALOY received FDA 510(k) clearance on 2003-11-12, under 510(k) number K033434.

Who is the listed applicant for BESTALOY?

The FDA 510(k) record lists We Dong Myung Dental Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BESTALOY?

The FDA product code for BESTALOY is EJJ.

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 We Dong Myung Dental Industrial Co., 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.

K033446APEX93, APEX87, APEX84, APEX85, APEX77, E-SARANG 88 AND E-SARANG 82K033435E-SARANG 86, DM78, DM55K030206APEX 90

Related Devices (Code: EJJ)

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.

K053114SILVERFILDunia Perwira Manufacturing Sdn. Bhd.K051010SECURALLOY, SEPTALLOY NG 50 AND SEPTALLOY NG 70SeptodontK032152BENCO ADMIXSouthern Dental Industries, Inc.K031658BENCO SPHERICALSouthern Dental Industries, Inc.K020452HIGH SILVER CONVENTIONALAb ArdentK011801FUTURA TOPCAP NON GAMMA-2Ab Ardent

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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