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FDA 510(k)

ORTHODONTIC FACE BOW W/ INNER WIRE

K-Number: K920784 · 1992-03-20

ApplicantGac Intl., Inc.
Decision Date1992-03-20
Product CodeDZB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORTHODONTIC FACE BOW W/ INNER WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Gac Intl., Inc.. It received FDA 510(k) clearance on 1992-03-20 under 510(k) number K920784. The device is classified under product code DZB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORTHODONTIC FACE BOW W/ INNER WIRE?

ORTHODONTIC FACE BOW W/ INNER WIRE is a medical device that received FDA 510(k) clearance on 1992-03-20. The listed applicant is Gac Intl., Inc.. The 510(k) number is K920784.

When did ORTHODONTIC FACE BOW W/ INNER WIRE receive FDA 510(k) clearance?

ORTHODONTIC FACE BOW W/ INNER WIRE received FDA 510(k) clearance on 1992-03-20, under 510(k) number K920784.

Who is the listed applicant for ORTHODONTIC FACE BOW W/ INNER WIRE?

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

What is the FDA product code for ORTHODONTIC FACE BOW W/ INNER WIRE?

The FDA product code for ORTHODONTIC FACE BOW W/ INNER WIRE is DZB.

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Related Devices (Code: DZB)

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.

K202855Orthodontic FacemaskIta.O Italian Orthodontic System S.R.L.K162543Reverse Pull Adjustable FacemaskSawbros Industries Pvt., Ltd.K111169PROTRACTION FACE MASK, REVERSE PULL FACE MASK MODEL KM-PVS, KM-PIS, KM-PVM, KM-PIM, MODEL KM-FMS, KM-FML, KM-FMFKwang Myung Daicom, Inc.K103019KJ MASKKj Meditech Co., Ltd.K052553NITOM LOCKING FACEBOWRussell Samuels Orthodontic DesignK051751EQUA-PULL SAFETY RELEASE MODULEOrtho Technology

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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