FDA 510(k)

EthanZir Zirconia

Número K: K191304 · 2019-11-04

RequerenteBesorah Dental Solutions NZ Limited

Data da decisão2019-11-04

Código do produtoEIH

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

EthanZir Zirconia is the device name listed in this FDA 510(k) record. The listed applicant is Besorah Dental Solutions NZ Limited. It received FDA 510(k) clearance on 2019-11-04 under 510(k) number K191304. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the EthanZir Zirconia?

EthanZir Zirconia is a medical device that received FDA 510(k) clearance on 2019-11-04. The listed applicant is Besorah Dental Solutions NZ Limited. The 510(k) number is K191304.

When did EthanZir Zirconia receive FDA 510(k) clearance?

EthanZir Zirconia received FDA 510(k) clearance on 2019-11-04, under 510(k) number K191304.

Who is the listed applicant for EthanZir Zirconia?

The FDA 510(k) record lists Besorah Dental Solutions NZ Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EthanZir Zirconia?

The FDA product code for EthanZir Zirconia is EIH.

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Dispositivos Relacionados (Código: EIH)

K262074Any-ZircosMediclus Co., Ltd.K262239Obsidian® Press Over ZirconiaPrismatik Dentalcraft, Inc.K261046Dental Zirconia Blank & Coloring LiquidHunan Qinghao Puzhong Technology Co., Ltd.K262195Dandy Ceramic Stain and GlazeZima International Inc., dba Dandy K260918Zolid LunarisAmann Girrbach AG K260859Rosetta SM, Rosetta SPHass Corp.

Fonte oficial

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