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FDA 510(k)

ORTHODONTIC ARCH

K-Number: K872622 · 1987-10-09

ApplicantWonder Wire
Decision Date1987-10-09
Product CodeEJZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORTHODONTIC ARCH is the device name listed in this FDA 510(k) record. The listed applicant is Wonder Wire. It received FDA 510(k) clearance on 1987-10-09 under 510(k) number K872622. The device is classified under product code EJZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHODONTIC ARCH?

ORTHODONTIC ARCH is a medical device that received FDA 510(k) clearance on 1987-10-09. The listed applicant is Wonder Wire. The 510(k) number is K872622.

When did ORTHODONTIC ARCH receive FDA 510(k) clearance?

ORTHODONTIC ARCH received FDA 510(k) clearance on 1987-10-09, under 510(k) number K872622.

Who is the listed applicant for ORTHODONTIC ARCH?

The FDA 510(k) record lists Wonder Wire as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORTHODONTIC ARCH?

The FDA product code for ORTHODONTIC ARCH is EJZ.

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 Wonder Wire 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.

K931631COATED ORTHODONTIC DEVICES

Related Devices (Code: EJZ)

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.

K823315DENTAL INSTRUMENTS - KNIVESMiltex, 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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