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FDA 510(k)

DPI-1106 IMPLANT, MODIFICATION

K-Number: K911776 · 1992-01-15

ApplicantMinimatic Implant Technology
Decision Date1992-01-15
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DPI-1106 IMPLANT, MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Minimatic Implant Technology. It received FDA 510(k) clearance on 1992-01-15 under 510(k) number K911776. 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 DPI-1106 IMPLANT, MODIFICATION?

DPI-1106 IMPLANT, MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-01-15. The listed applicant is Minimatic Implant Technology. The 510(k) number is K911776.

When did DPI-1106 IMPLANT, MODIFICATION receive FDA 510(k) clearance?

DPI-1106 IMPLANT, MODIFICATION received FDA 510(k) clearance on 1992-01-15, under 510(k) number K911776.

Who is the listed applicant for DPI-1106 IMPLANT, MODIFICATION?

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

What is the FDA product code for DPI-1106 IMPLANT, MODIFICATION?

The FDA product code for DPI-1106 IMPLANT, MODIFICATION is DZE.

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Other records listing Minimatic Implant Technology 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.

K903515HH-1119 HEALING HEADK911112DEVICE PART NUMBERS: - 1400 SERIESK905039IMPLANT, THREADED EXTERNAL HEX, TAPERED SHOULDERK904707BC 1208 IMPLANT, THREADED EXTERNAL HEXK903043ICT-1108 IMPLANT- THREADED (CEMENT TYPE ABUTMENT)K903046IDT-1104 IMPLANT (SCREW-IN-THREADED)

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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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