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FDA 510(k)

DISCARD DENTAL EXPLORER

K-Number: K885217 · 1989-01-19

ApplicantWen Hao, Inc.
Decision Date1989-01-19
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DISCARD DENTAL EXPLORER is the device name listed in this FDA 510(k) record. The listed applicant is Wen Hao, Inc.. It received FDA 510(k) clearance on 1989-01-19 under 510(k) number K885217. The device is classified under product code EKJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISCARD DENTAL EXPLORER?

DISCARD DENTAL EXPLORER is a medical device that received FDA 510(k) clearance on 1989-01-19. The listed applicant is Wen Hao, Inc.. The 510(k) number is K885217.

When did DISCARD DENTAL EXPLORER receive FDA 510(k) clearance?

DISCARD DENTAL EXPLORER received FDA 510(k) clearance on 1989-01-19, under 510(k) number K885217.

Who is the listed applicant for DISCARD DENTAL EXPLORER?

The FDA 510(k) record lists Wen Hao, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISCARD DENTAL EXPLORER?

The FDA product code for DISCARD DENTAL EXPLORER is EKJ.

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 Wen Hao, Inc. 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.

K893027PATIENT EXAM GLOVES (MFG JET FAR INDU. INC.)K893025EXAM GLOVES (MFG. GUEY HER ENT. CO. LTD)K885219DENTAL DRESSING PLIERSK885218DISCARD DENTAL MIRROR

Related Devices (Code: EKJ)

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.

K961714ASEPTYLUM, UNI-CARRIERDistriflor S.A.K953707MEDTROL DENTAL KITMedtrol, Inc.K945815DENTAL KITConstancy Ent., Inc.K951607SUREFLEX FILESDentsply Intl.K945077INSTRUMENT,FILLING,PLASTIC,DENTALWorldwide Dental, Inc.K943820STAT PAKMagnum Instruments, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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