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FDA 510(k)

ORTHODONTIC BRACKET/SPEED/HANSON SPEED

K-Number: K801809 · 1980-08-13

Decision Date1980-08-13
Product CodeEJF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORTHODONTIC BRACKET/SPEED/HANSON SPEED is the device name listed in this FDA 510(k) record. The listed applicant is Strite Industries , Ltd.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801809. 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 ORTHODONTIC BRACKET/SPEED/HANSON SPEED?

ORTHODONTIC BRACKET/SPEED/HANSON SPEED is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Strite Industries , Ltd.. The 510(k) number is K801809.

When did ORTHODONTIC BRACKET/SPEED/HANSON SPEED receive FDA 510(k) clearance?

ORTHODONTIC BRACKET/SPEED/HANSON SPEED received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801809.

Who is the listed applicant for ORTHODONTIC BRACKET/SPEED/HANSON SPEED?

The FDA 510(k) record lists Strite Industries , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ORTHODONTIC BRACKET/SPEED/HANSON SPEED?

The FDA product code for ORTHODONTIC BRACKET/SPEED/HANSON SPEED is EJF.

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.

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.

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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