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FDA 510(k)

.016' X .016 NICKEL TITANIUM UPRIGHTING SPRING

K-Number: K923836 · 1992-12-23

ApplicantUltimate Wireforms, Inc.
Decision Date1992-12-23
Product CodeDZC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

.016' X .016 NICKEL TITANIUM UPRIGHTING SPRING 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 1992-12-23 under 510(k) number K923836. 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 .016' X .016 NICKEL TITANIUM UPRIGHTING SPRING?

.016' X .016 NICKEL TITANIUM UPRIGHTING SPRING is a medical device that received FDA 510(k) clearance on 1992-12-23. The listed applicant is Ultimate Wireforms, Inc.. The 510(k) number is K923836.

When did .016' X .016 NICKEL TITANIUM UPRIGHTING SPRING receive FDA 510(k) clearance?

.016' X .016 NICKEL TITANIUM UPRIGHTING SPRING received FDA 510(k) clearance on 1992-12-23, under 510(k) number K923836.

Who is the listed applicant for .016' X .016 NICKEL TITANIUM UPRIGHTING SPRING?

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 .016' X .016 NICKEL TITANIUM UPRIGHTING SPRING?

The FDA product code for .016' X .016 NICKEL TITANIUM UPRIGHTING SPRING is DZC.

Related Clinical Trials

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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 WIREK923837DIMPLED MULTI MODULUS ARCH WIREK923838THE 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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