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FDA 510(k)

DYNA IMPLANT DESIGN

K-Number: K930868 · 1995-04-28

ApplicantDyna Dental Engineering BV
Decision Date1995-04-28
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DYNA IMPLANT DESIGN is the device name listed in this FDA 510(k) record. The listed applicant is Dyna Dental Engineering BV. It received FDA 510(k) clearance on 1995-04-28 under 510(k) number K930868. 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 DYNA IMPLANT DESIGN?

DYNA IMPLANT DESIGN is a medical device that received FDA 510(k) clearance on 1995-04-28. The listed applicant is Dyna Dental Engineering BV. The 510(k) number is K930868.

When did DYNA IMPLANT DESIGN receive FDA 510(k) clearance?

DYNA IMPLANT DESIGN received FDA 510(k) clearance on 1995-04-28, under 510(k) number K930868.

Who is the listed applicant for DYNA IMPLANT DESIGN?

The FDA 510(k) record lists Dyna Dental Engineering BV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DYNA IMPLANT DESIGN?

The FDA product code for DYNA IMPLANT DESIGN is DZE.

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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

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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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