AHL GENERIC GLASS IONOMER AESTHETIC RESTORATIVE— 510(k) K020376

Name: FDA 510(k) clearance K020376
Creator: U.S. Food and Drug Administration
Published: 2002-04-09

Substantially Equivalent

Advanced Healthcare , Ltd.

FDA 510(k) clearance K020376 for AHL GENERIC GLASS IONOMER AESTHETIC RESTORATIVE, Substantially Equivalent on 2002-04-09. Applicant: Advanced Healthcare , Ltd.. Device class: 2.

Clearance details

Applicant: Advanced Healthcare , Ltd.
Product code: Code EMA
Device class: Class 2
Regulation: 21 CFR 872.3275
Advisory panel: Dental
Date received: 2002-02-04
Decision date: 2002-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sylmar, CA, 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 Advanced Healthcare , Ltd.

view all

K024287 — FIXOBRIDGE 3-CEMENT2003-03-21
K023981 — AHL GENERIC GLASS IONOMER LUTING CEMENT2003-01-31

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