FDA 510(k)

C&B NFH Hybrid

K-Number: K232559 · 2024-09-11

Decision Date2024-09-11

Product CodeEBF

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

C&B NFH Hybrid is a medical device manufactured by Arum Dentistry Co., Ltd.. It received FDA 510(k) clearance on 2024-09-11 under approval number K232559. 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 C&B NFH Hybrid?

C&B NFH Hybrid is a medical device that received FDA 510(k) clearance on 2024-09-11. It is manufactured by Arum Dentistry Co., Ltd.. The 510(k) number is K232559.

When was C&B NFH Hybrid approved by the FDA?

C&B NFH Hybrid received FDA 510(k) clearance on 2024-09-11, under approval number K232559.

What company makes C&B NFH Hybrid?

C&B NFH Hybrid is manufactured by Arum Dentistry Co., Ltd..

What is the FDA product code for C&B NFH Hybrid?

The FDA product code for C&B NFH Hybrid is EBF.

Other Devices by Arum Dentistry Co., Ltd.

K193425Pre-Milled Blank K210817C&B 5.0 Hybrid K222131NB 1 SA Implant System K213506NB 1 SA Implant System K232560Angled Abutment K230725NB Implant System

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Related Devices (Code: EBF)

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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.