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FDA 510(k)

DIMPLED MULTI MODULUS ARCH WIRE

K-Number: K923837 · 1993-03-31

ApplicantUltimate Wireforms, Inc.
Decision Date1993-03-31
Product CodeDZC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DIMPLED MULTI MODULUS ARCH WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Ultimate Wireforms, Inc.. It received FDA 510(k) clearance on 1993-03-31 under 510(k) number K923837. The device is classified under product code DZC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIMPLED MULTI MODULUS ARCH WIRE?

DIMPLED MULTI MODULUS ARCH WIRE is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is Ultimate Wireforms, Inc.. The 510(k) number is K923837.

When did DIMPLED MULTI MODULUS ARCH WIRE receive FDA 510(k) clearance?

DIMPLED MULTI MODULUS ARCH WIRE received FDA 510(k) clearance on 1993-03-31, under 510(k) number K923837.

Who is the listed applicant for DIMPLED MULTI MODULUS ARCH WIRE?

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

What is the FDA product code for DIMPLED MULTI MODULUS ARCH WIRE?

The FDA product code for DIMPLED MULTI MODULUS ARCH WIRE is DZC.

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 Ultimate Wireforms, 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.

K960799ORTHO-ICEK924805ORTHODONTIC ARCH WIREK923836.016' X .016 NICKEL TITANIUM UPRIGHTING SPRINGK923838THE ULTIMATE RCS ARCH WIREK923839NITINOL GENTLE TOUCH COIL SPRING

Related Devices (Code: DZC)

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.

K112640HYPERELASTIC WIREOrmco Corp.K943334HAWLEY RETAINER ORTHODONTIC APPLICANCE KITJay H. GellerK935638NITINOL, NITIHighland MetalsK935140DENTAURUM STEEL LIGATURE WIRESDentauraum, Inc.K935142DENTAURUM WIRESDentauraum, Inc.K934265FLEXMEDICS SUPER-SEVEN STRANDED NICKEL-TITANIUM ARCHWIREFlexmedics

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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