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FDA 510(k)

FACEBOW

K-Number: K925240 · 1993-06-18

ApplicantForestadent Bernhard Forster GmbH
Decision Date1993-06-18
Product CodeDZB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FACEBOW is the device name listed in this FDA 510(k) record. The listed applicant is Forestadent Bernhard Forster GmbH. It received FDA 510(k) clearance on 1993-06-18 under 510(k) number K925240. 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 FACEBOW?

FACEBOW is a medical device that received FDA 510(k) clearance on 1993-06-18. The listed applicant is Forestadent Bernhard Forster GmbH. The 510(k) number is K925240.

When did FACEBOW receive FDA 510(k) clearance?

FACEBOW received FDA 510(k) clearance on 1993-06-18, under 510(k) number K925240.

Who is the listed applicant for FACEBOW?

The FDA 510(k) record lists Forestadent Bernhard Forster GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FACEBOW?

The FDA product code for FACEBOW is DZB.

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Other records listing Forestadent Bernhard Forster GmbH 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.

K110275ORTHO EASY PINK090933BERNHARD-FORSTER GMBH ORTHODONTIC CERAMIC BRACKETSK924971FORESTADENT BRACKETS

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

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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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