FUTURABOND UNIVERSAL— 510(k) K130486

Substantially Equivalent

Voco GmbH

FDA 510(k) clearance K130486 for FUTURABOND UNIVERSAL, Substantially Equivalent on 2013-06-20. Applicant: Voco GmbH. Device class: 2.

Clearance details

Applicant: Voco GmbH
Product code: Code KLE
Device class: Class 2
Regulation: 21 CFR 872.3200
Advisory panel: Dental
Date received: 2013-02-25
Decision date: 2013-06-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cuxhaven, DE

Download summary PDF View on FDA.gov ↗

Recent devices under product code KLE

K260485 — Any-Etch2026-05-14
K260430 — Porcelain Etch Gel2026-04-10
K252450 — Adhese 22026-03-05
K260682 — Bond-PR Universal Adhesive2026-03-03
K251587 — VITA VMLC Primer2026-02-23

More clearances from Voco GmbH

K252073 — VOCO Profluorid Varnish + BioMin2026-05-01
K261357 — Grandio disc multicolor2026-04-27
K252606 — Bifix Veneer LC, Bifix Veneer Try-In2026-03-20
K251390 — MTA vpt2025-07-03
K251239 — GrandioSO Unlimited2025-05-21

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