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FDA 510(k)

FRANCE ORTHODONTIE

K-Number: K950121 · 1995-03-08

ApplicantFrance Orthodontie
Decision Date1995-03-08
Product CodeDZB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FRANCE ORTHODONTIE is the device name listed in this FDA 510(k) record. The listed applicant is France Orthodontie. It received FDA 510(k) clearance on 1995-03-08 under 510(k) number K950121. 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 FRANCE ORTHODONTIE?

FRANCE ORTHODONTIE is a medical device that received FDA 510(k) clearance on 1995-03-08. The listed applicant is France Orthodontie. The 510(k) number is K950121.

When did FRANCE ORTHODONTIE receive FDA 510(k) clearance?

FRANCE ORTHODONTIE received FDA 510(k) clearance on 1995-03-08, under 510(k) number K950121.

Who is the listed applicant for FRANCE ORTHODONTIE?

The FDA 510(k) record lists France Orthodontie as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FRANCE ORTHODONTIE?

The FDA product code for FRANCE ORTHODONTIE 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

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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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