FDA 510(k)

BTI Interna Dental Implant System UnicCa - Prosthetic Components

Número K: K213106 · 2022-10-20

RequerenteB.T.I. Biotechnology Institute, Sl.

Data da decisão2022-10-20

Código do produtoNHA

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

BTI Interna Dental Implant System UnicCa - Prosthetic Components is the device name listed in this FDA 510(k) record. The listed applicant is B.T.I. Biotechnology Institute, Sl.. It received FDA 510(k) clearance on 2022-10-20 under 510(k) number K213106. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the BTI Interna Dental Implant System UnicCa - Prosthetic Components?

BTI Interna Dental Implant System UnicCa - Prosthetic Components is a medical device that received FDA 510(k) clearance on 2022-10-20. The listed applicant is B.T.I. Biotechnology Institute, Sl.. The 510(k) number is K213106.

When did BTI Interna Dental Implant System UnicCa - Prosthetic Components receive FDA 510(k) clearance?

BTI Interna Dental Implant System UnicCa - Prosthetic Components received FDA 510(k) clearance on 2022-10-20, under 510(k) number K213106.

Who is the listed applicant for BTI Interna Dental Implant System UnicCa - Prosthetic Components?

The FDA 510(k) record lists B.T.I. Biotechnology Institute, Sl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BTI Interna Dental Implant System UnicCa - Prosthetic Components?

The FDA product code for BTI Interna Dental Implant System UnicCa - Prosthetic Components is NHA.

Ensaios clínicos relacionados

Registros relacionados são pareados automaticamente usando nomes, códigos de produtos ou outros metadados. Um pareamento não estabelece um vínculo clínico, científico, corporativo ou regulatório verificado; revise as fontes oficiais vinculadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Outros registros que listam B.T.I. Biotechnology Institute, Sl. como candidato(a)

K240262BTI Interna 3.0 Dental Implant System UnicCa®K232750BTI Interna Prosthetic Components K231827BTI Dental Implant System UnicCa® – Aesthetic Post Abutments K211952BTI Interna Narrow/Plus Dental Implant System UnicCa K202825BTI Extra-Short Dental Implant System UnicCa K173257BTI Dental Implant System UnicCa

Ver todos os 8 dispositivos →

Dispositivos Relacionados (Código: NHA)

K262207Cemented Plus AbutmentUnidental Co., Ltd.K260940BellaTek BarsZimVie US Corp, LLC K253999Universal Base ASC Engaging; Universal Base ASC Non-Engaging; Universal Base MUA ASC; Temporary Abutment Engaging and Non-Engaging; Healing Abutment Conical Connection; Omnigrip Clinical Screw Titanium; Omnigrip Prosthetic ScrewNobel Biocare AB K261147Neodent Implant System - NeoConvert FitJJGC Indústria e Comércio de Materiais Dentários S.A.K261122MIST ICImagine Milling Technologies, LLC K260061BioHorizons CEREC Compatible Ti-BasesBioHorizons Implant Systems, Inc.

Fonte oficial

Ver na base de dados da FDA →

Dados provenientes da FDA Open API. Para informações mais recentes e oficiais, consulte sempre o registro oficial.