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FDA 510(k)

RELIANCE SHORT STICK TIE

K-Number: K925712 · 1993-01-11

Decision Date1993-01-11
Product CodeDYX
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RELIANCE SHORT STICK TIE is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Orthodontic Products, Inc.. It received FDA 510(k) clearance on 1993-01-11 under 510(k) number K925712. The device is classified under product code DYX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RELIANCE SHORT STICK TIE?

RELIANCE SHORT STICK TIE is a medical device that received FDA 510(k) clearance on 1993-01-11. The listed applicant is Reliance Orthodontic Products, Inc.. The 510(k) number is K925712.

When did RELIANCE SHORT STICK TIE receive FDA 510(k) clearance?

RELIANCE SHORT STICK TIE received FDA 510(k) clearance on 1993-01-11, under 510(k) number K925712.

Who is the listed applicant for RELIANCE SHORT STICK TIE?

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

What is the FDA product code for RELIANCE SHORT STICK TIE?

The FDA product code for RELIANCE SHORT STICK TIE is DYX.

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.

Other records listing Reliance Orthodontic Products, 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.

View all 32 devices →

Related Devices (Code: DYX)

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

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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