Stasis Gel— 510(k) K211420

Name: FDA 510(k) clearance K211420
Creator: U.S. Food and Drug Administration
Published: 2022-03-14

Substantially Equivalent

Belport Company, Inc., Gingi-Pak

FDA 510(k) clearance K211420 for Stasis Gel, Substantially Equivalent on 2022-03-14. Applicant: Belport Company, Inc., Gingi-Pak. Device class: Unclassified.

Clearance details

Applicant: Belport Company, Inc., Gingi-Pak
Product code: Product code MVL
Device class: Unclassified
Advisory panel: Unknown
Date received: 2021-05-07
Decision date: 2022-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MVL

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K253797 — One-Stop2026-02-27
K243910 — Retraxil2025-09-24
K211419 — Gingi-Aid Gel2022-01-10
K213149 — VOCO Retraction Paste2021-12-09

More clearances from Belport Company, Inc., Gingi-Pak

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K240688 — RODIN Titan 3D Resin2024-06-20

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