ALPHA-DENT LIGHT ACTIVATED CORE BUILDUP BLUE PASTE— 510(k) K932886

Name: FDA 510(k) clearance K932886
Creator: U.S. Food and Drug Administration
Published: 1993-09-29

Substantially Equivalent

Wallace A. Erickson & Co.

FDA 510(k) clearance K932886 for ALPHA-DENT LIGHT ACTIVATED CORE BUILDUP BLUE PASTE, Substantially Equivalent on 1993-09-29. Applicant: Wallace A. Erickson & Co.. Device class: 2.

Clearance details

Applicant: Wallace A. Erickson & Co.
Product code: Code EBF
Device class: Class 2
Regulation: 21 CFR 872.3690
Advisory panel: Dental
Date received: 1993-06-14
Decision date: 1993-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EBF

view all

K262202 — Cerasmart Forte2026-09-10
K261695 — Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)2026-08-31
K261485 — Tetric plus Fill; Tetric plus Flow2026-07-01
K262228 — Transcend Bulk Fill Flowable Composite2026-07-01
K261246 — SRGC-062026-06-18

More clearances from Wallace A. Erickson & Co.

view all

K984503 — ALPHA BOND DENTIN/ENAMEL BONDING AGENT, MODEL 213-0001999-02-26
K963922 — ALPHA-DENT ROOT CANAL SEALER & FILLER1996-12-06
K960667 — CENTRIX FLOFIL/CENTRIX FLOFIL WITH FLUORIDE1996-07-02
K960365 — ALPHA-DENT HEMA DESENTIZER(748-000)/WITH FLUORIDE(747-000)1996-03-28
K960165 — ALPHA-DENT COMPOSITE SURFACE SEALANT1996-03-15

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