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FDA 510(k)

DISCARD DENTAL MIRROR

K-Number: K885218 · 1989-01-19

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

Device Summary

DISCARD DENTAL MIRROR 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 K885218. 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 MIRROR?

DISCARD DENTAL MIRROR 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 K885218.

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

DISCARD DENTAL MIRROR received FDA 510(k) clearance on 1989-01-19, under 510(k) number K885218.

Who is the listed applicant for DISCARD DENTAL MIRROR?

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 MIRROR?

The FDA product code for DISCARD DENTAL MIRROR 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)K885217DISCARD DENTAL EXPLORERK885219DENTAL DRESSING PLIERS

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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