VioSeal
K-Number: K242702 · 2024-11-07
Device Summary
Frequently Asked Questions
What is the VioSeal?
VioSeal is a medical device that received FDA 510(k) clearance on 2024-11-07. The listed applicant is Spident Co., Ltd.. The 510(k) number is K242702.
When did VioSeal receive FDA 510(k) clearance?
VioSeal received FDA 510(k) clearance on 2024-11-07, under 510(k) number K242702.
Who is the listed applicant for VioSeal?
The FDA 510(k) record lists Spident Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VioSeal?
The FDA product code for VioSeal is KIF.
Other records listing Spident Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KIF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.