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FDA 510(k)

HALL ORAL IMPLANT SYSTEM

K-Number: K864734 · 1987-02-10

ApplicantHall Surgical, Division of Zimmer, Inc.
Decision Date1987-02-10
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HALL ORAL IMPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Hall Surgical, Division of Zimmer, Inc.. It received FDA 510(k) clearance on 1987-02-10 under 510(k) number K864734. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HALL ORAL IMPLANT SYSTEM?

HALL ORAL IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 1987-02-10. The listed applicant is Hall Surgical, Division of Zimmer, Inc.. The 510(k) number is K864734.

When did HALL ORAL IMPLANT SYSTEM receive FDA 510(k) clearance?

HALL ORAL IMPLANT SYSTEM received FDA 510(k) clearance on 1987-02-10, under 510(k) number K864734.

Who is the listed applicant for HALL ORAL IMPLANT SYSTEM?

The FDA 510(k) record lists Hall Surgical, Division of Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HALL ORAL IMPLANT SYSTEM?

The FDA product code for HALL ORAL IMPLANT SYSTEM is DZE.

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Other records listing Hall Surgical, Division of Zimmer, 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.

K942660HALL MICROCHOICE ELECTRIC POWERED SYSTEMK864929HALL (R) MICRO E POWERED SURGICAL INSTRUMENT SYSTK864163HALL DUNBAR DRILL GUIDE SYSTEMK862778HALL CANNLULA SYSTEMK862474HALL STERNUM SAWK862529HALL STERILE BUR

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Related Devices (Code: DZE)

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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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