3M VITREMER TRI-CURE GLASS IONOMER SYSTEM— 510(k) K925032

Name: FDA 510(k) clearance K925032
Creator: U.S. Food and Drug Administration
Published: 1992-12-23

Substantially Equivalent

3M Company

FDA 510(k) clearance K925032 for 3M VITREMER TRI-CURE GLASS IONOMER SYSTEM, Substantially Equivalent on 1992-12-23. Applicant: 3M Company. Device class: 2.

Clearance details

Applicant: 3M Company
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 1992-10-05
Decision date: 1992-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cottae Grove, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EMA

view all

K254201 — Any-Cem2026-08-13
K261937 — PacTemp Automix NE2026-08-07
K261166 — DIA-CEM2026-07-09
K254109 — G-CEM UNIVERSAL2026-05-18
K253337 — REGEN Bioactive Cement2026-04-15

More clearances from 3M Company

view all

K243501 — 3M Attest Super Rapid Steam Extended Cycle Clear Challenge Pack 1492PCDE +3 more2025-01-28
K242538 — 3M Attest Super Rapid Readout Biological Indicator 1493 +4 more2024-11-25
K241959 — 3M Attest Super Rapid Steam Clear Challenge Pack (1492PCD) +3 more2024-10-18
K241710 — 3M Attest Super Rapid Readout Biological Indicator 1492V +3 more2024-09-12
K240717 — 3M Attest Rapid Readout Biological Indicator 1295 and 3M Attest Vaporized Hydrogen Peroxide Tri-Metric Chemical Indicator 1348/1348E2024-06-27

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