FDA 510(k)

Injectable Root Canal Bioceramic Sealer (NR SP-0.5, NR SP-1, NR SP-2, NR SP-3, NR SP-5)

Número K: K240304 · 2024-05-28

RequerenteEnpuno Biotechnology Co., Ltd.

Data da decisão2024-05-28

Código do produtoKIF

Comité consultivoDE

DecisãoSubstantially Equivalent

Resumo do dispositivo

Injectable Root Canal Bioceramic Sealer (NR SP-0.5, NR SP-1, NR SP-2, NR SP-3, NR SP-5) is the device name listed in this FDA 510(k) record. The listed applicant is Enpuno Biotechnology Co., Ltd.. It received FDA 510(k) clearance on 2024-05-28 under 510(k) number K240304. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Injectable Root Canal Bioceramic Sealer (NR SP-0.5, NR SP-1, NR SP-2, NR SP-3, NR SP-5)?

Injectable Root Canal Bioceramic Sealer (NR SP-0.5, NR SP-1, NR SP-2, NR SP-3, NR SP-5) is a medical device that received FDA 510(k) clearance on 2024-05-28. The listed applicant is Enpuno Biotechnology Co., Ltd.. The 510(k) number is K240304.

When did Injectable Root Canal Bioceramic Sealer (NR SP-0.5, NR SP-1, NR SP-2, NR SP-3, NR SP-5) receive FDA 510(k) clearance?

Injectable Root Canal Bioceramic Sealer (NR SP-0.5, NR SP-1, NR SP-2, NR SP-3, NR SP-5) received FDA 510(k) clearance on 2024-05-28, under 510(k) number K240304.

Who is the listed applicant for Injectable Root Canal Bioceramic Sealer (NR SP-0.5, NR SP-1, NR SP-2, NR SP-3, NR SP-5)?

The FDA 510(k) record lists Enpuno Biotechnology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Injectable Root Canal Bioceramic Sealer (NR SP-0.5, NR SP-1, NR SP-2, NR SP-3, NR SP-5)?

The FDA product code for Injectable Root Canal Bioceramic Sealer (NR SP-0.5, NR SP-1, NR SP-2, NR SP-3, NR SP-5) is KIF.

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Fonte oficial

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