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FDA 510(k)

X-RING AND SPEED STIX PLASTIC LIGATURES

K-Number: K893555 · 1989-07-14

ApplicantAmerican Orthodontics
Decision Date1989-07-14
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

X-RING AND SPEED STIX PLASTIC LIGATURES is the device name listed in this FDA 510(k) record. The listed applicant is American Orthodontics. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K893555. The device is classified under product code EJF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-RING AND SPEED STIX PLASTIC LIGATURES?

X-RING AND SPEED STIX PLASTIC LIGATURES is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is American Orthodontics. The 510(k) number is K893555.

When did X-RING AND SPEED STIX PLASTIC LIGATURES receive FDA 510(k) clearance?

X-RING AND SPEED STIX PLASTIC LIGATURES received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893555.

Who is the listed applicant for X-RING AND SPEED STIX PLASTIC LIGATURES?

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 X-RING AND SPEED STIX PLASTIC LIGATURES?

The FDA product code for X-RING AND SPEED STIX PLASTIC LIGATURES is EJF.

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Related Devices (Code: EJF)

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.

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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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