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FDA 510(k)

POST. SCREW & HEX DRIVER/ADBUT & ADBUT HEAD DRIVER

K-Number: K871862 · 1987-07-10

ApplicantImplant Innovations International, Inc.
Decision Date1987-07-10
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POST. SCREW & HEX DRIVER/ADBUT & ADBUT HEAD DRIVER is the device name listed in this FDA 510(k) record. The listed applicant is Implant Innovations International, Inc.. It received FDA 510(k) clearance on 1987-07-10 under 510(k) number K871862. 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 POST. SCREW & HEX DRIVER/ADBUT & ADBUT HEAD DRIVER?

POST. SCREW & HEX DRIVER/ADBUT & ADBUT HEAD DRIVER is a medical device that received FDA 510(k) clearance on 1987-07-10. The listed applicant is Implant Innovations International, Inc.. The 510(k) number is K871862.

When did POST. SCREW & HEX DRIVER/ADBUT & ADBUT HEAD DRIVER receive FDA 510(k) clearance?

POST. SCREW & HEX DRIVER/ADBUT & ADBUT HEAD DRIVER received FDA 510(k) clearance on 1987-07-10, under 510(k) number K871862.

Who is the listed applicant for POST. SCREW & HEX DRIVER/ADBUT & ADBUT HEAD DRIVER?

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

What is the FDA product code for POST. SCREW & HEX DRIVER/ADBUT & ADBUT HEAD DRIVER?

The FDA product code for POST. SCREW & HEX DRIVER/ADBUT & ADBUT HEAD DRIVER is DZE.

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Other records listing Implant Innovations International, 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.

K9355443I STANDARD THREADED/SELF-TAPPING THREADED IMPLANTS MODIFICATIONK932123IMPLANT INNOVATION PRE-ANGLED ABUTMENT SYSTEMK911655IMPLARETTEK905303ABUTMENT GLOK911701G-FLOSS & G-FLOSS IIK891613OVERDENTURE ATTACHMENT

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Related Devices (Code: DZE)

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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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