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FDA 510(k)

UNI-STICK PLASTIC LIGATURE, MODIFIED

K-Number: K926578 · 1993-03-31

ApplicantAmerican Orthodontics
Decision Date1993-03-31
Product CodeECI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UNI-STICK PLASTIC LIGATURE, MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is American Orthodontics. It received FDA 510(k) clearance on 1993-03-31 under 510(k) number K926578. The device is classified under product code ECI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNI-STICK PLASTIC LIGATURE, MODIFIED?

UNI-STICK PLASTIC LIGATURE, MODIFIED is a medical device that received FDA 510(k) clearance on 1993-03-31. The listed applicant is American Orthodontics. The 510(k) number is K926578.

When did UNI-STICK PLASTIC LIGATURE, MODIFIED receive FDA 510(k) clearance?

UNI-STICK PLASTIC LIGATURE, MODIFIED received FDA 510(k) clearance on 1993-03-31, under 510(k) number K926578.

Who is the listed applicant for UNI-STICK PLASTIC LIGATURE, MODIFIED?

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

What is the FDA product code for UNI-STICK PLASTIC LIGATURE, MODIFIED?

The FDA product code for UNI-STICK PLASTIC LIGATURE, MODIFIED is ECI.

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Other records listing American Orthodontics as applicant

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Related Devices (Code: ECI)

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.

K980864POWER COINS GLOW IN THE DARK LIGATURESOrtho Kinetics Corp.K980053GLENROE CHAINGlenroe TechnologiesK973495GLENROE GLOW IN DARK ELASTOMERIC LIGATURESGlenroeK943419ORTHODONTIC ELASTOMERIC LAGATURE MODULEJon-Ko Products, Inc.K943420ORTHODONTIC ELASTOMERIC CHAINJon-Ko Products, Inc.K943418ORTHODONTIC ELASTOMERIC SEPARATOR MODULEJon-Ko Products, Inc.

Official Source

View on FDA Database →

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

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