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FDA 510(k)

VioSeal

K-Number: K242702 · 2024-11-07

ApplicantSpident Co., Ltd.
Decision Date2024-11-07
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VioSeal is a medical device manufactured by Spident Co., Ltd.. It received FDA 510(k) clearance on 2024-11-07 under approval number K242702. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VioSeal?

VioSeal is a medical device that received FDA 510(k) clearance on 2024-11-07. It is manufactured by Spident Co., Ltd.. The 510(k) number is K242702.

When was VioSeal approved by the FDA?

VioSeal received FDA 510(k) clearance on 2024-11-07, under approval number K242702.

What company makes VioSeal?

VioSeal is manufactured by Spident Co., Ltd..

What is the FDA product code for VioSeal?

The FDA product code for VioSeal is KIF.

Other Devices by Spident Co., Ltd.

K161774i-Sil K214076EsCem K214071Hexa-Temp K231523EsCom250 K242675FineEtch (FineEtch-10 1.2ml, FineEtch-10 5ml, FineEtch-37 1.2ml FineEtch-37 5ml, FineEtch 37% 1.2ml 20ea pack) K241445K-Bond Universal

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Related Devices (Code: KIF)

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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.

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