VioSeal— 510(k) K242702

Substantially Equivalent

Spident Co., Ltd.

FDA 510(k) clearance K242702 for VioSeal, Substantially Equivalent on 2024-11-07. Applicant: Spident Co., Ltd.. Device class: 2.

Clearance details

Applicant: Spident Co., Ltd.
Product code: Code KIF
Device class: Class 2
Regulation: 21 CFR 872.3820
Advisory panel: Dental
Date received: 2024-09-09
Decision date: 2024-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Incheon, KR

Download summary PDF View on FDA.gov ↗

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K261415 — Injectable Root Canal Sealer (KP-Root SP)2026-06-29
K253167 — Any-Paste2026-01-12

More clearances from Spident Co., Ltd.

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K241445 — K-Bond Universal2024-07-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.