510(k) Report

FDA applicant

Dental Ventures of America, Inc.

Mchenry, IL3 decisions1978–20000 recalls

FDA records 3 decisions for Dental Ventures of America, Inc. (Mchenry, IL) from 1978 to 2000: 3 510(k) clearances. Most are in product codes EJH (Alloy, Metal, Base) and ELC (Scaler, Ultrasonic). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Dental Ventures of America, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dental Ventures of America, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dental Ventures of America, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • EJHAlloy, Metal, Base1decision
  • ELCScaler, Ultrasonic1decision
  • EBGCrown And Bridge, Temporary, Resin1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K000894C&B Resin Plus Powder/Liquid, Models Retemp A2, A3, A3.5, CL, Retemp B2, B3, C2, D3, WH, Retemp MODental Ventures of America, Inc. · 20001cites it

What has FDA decided for it lately?

  • K000894C&B Resin Plus Powder/Liquid, Models Retemp A2, A3, A3.5, CL, Retemp B2, B3, C2, D3, WH, Retemp MODental Ventures of America, Inc. · 2000
  • K842377MS Nonprecious Crown & Bridge AlloyDental Ventures of America, Inc. · 1984
  • K780808Piezomatic Ultrasonic Scaler (System S)Dental Ventures of America, Inc. · 1978

All 3 as Dental Ventures of America, Inc. →