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FDA 510(k)

VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM

K-Number: K961434 · 1996-07-08

ApplicantVident
Decision Date1996-07-08
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Vident. It received FDA 510(k) clearance on 1996-07-08 under 510(k) number K961434. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM?

VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM is a medical device that received FDA 510(k) clearance on 1996-07-08. The listed applicant is Vident. The 510(k) number is K961434.

When did VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM receive FDA 510(k) clearance?

VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM received FDA 510(k) clearance on 1996-07-08, under 510(k) number K961434.

Who is the listed applicant for VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM?

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

What is the FDA product code for VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM?

The FDA product code for VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM is EBF.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Vident 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.

K063768TITANIUM SCALLOPED ABUTMENTK060441VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9, MODEL NX98K052710VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,K052130VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40K050362VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)K022996VITA IN-CERAM YZ CUBES FOR CEREC

View all 36 devices →

Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, 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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