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FDA 510(k)

ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM

K-Number: K011245 · 2001-06-25

ApplicantSulzer Dental, Inc.
Decision Date2001-06-25
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sulzer Dental, Inc.. It received FDA 510(k) clearance on 2001-06-25 under 510(k) number K011245. 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 ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM?

ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM is a medical device that received FDA 510(k) clearance on 2001-06-25. The listed applicant is Sulzer Dental, Inc.. The 510(k) number is K011245.

When did ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM receive FDA 510(k) clearance?

ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM received FDA 510(k) clearance on 2001-06-25, under 510(k) number K011245.

Who is the listed applicant for ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM?

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

What is the FDA product code for ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM?

The FDA product code for ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM is DZE.

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Other records listing Sulzer Dental, 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.

K014050HEX-LOCK TEMPORARY ABUTMENTK014175SULZER DENTAL CERAMIC SYSTEM-HEXLOCKK014214SULZER DENTAL CERAMIC SYSTEM-SPLINEK0134943.75MM AND 5.0MM SPLINE TWIST IMPLANTK013227SCREW VENT IMPLANT; TAPERED SCREW VENT IMPLANTK0120553.25MM SPLINE TWIST IMPLANT

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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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