510(k) Report

FDA applicant

Minnesota Prophy Power, Inc.

Lakeville, MN2 decisions1994–19940 recalls

FDA records 2 decisions for Minnesota Prophy Power, Inc. (Lakeville, MN) in 1994: 2 510(k) clearances. Most are in product codes EMN (Scaler, Periodontic) and EMS (Curette, Periodontic). 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 Minnesota Prophy Power, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Minnesota Prophy Power, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Minnesota Prophy Power, 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?

  • EMNScaler, Periodontic1decision
  • EMSCurette, Periodontic1decision

What has FDA decided for it lately?

  • K931329Dental Instruments Curette PeriodontalMinnesota Prophy Power, Inc. · 1994
  • K931330Dental Instruments ScalerMinnesota Prophy Power, Inc. · 1994

All 2 as Minnesota Prophy Power, Inc. →

Other applicant names beginning “Minnesota”

FDA records each applicant name separately; these may or may not be the same firm.

Minnesota Laser Corp. 12Minnesota Mining and Mfg. Co. 9Minnesota Scientific, Inc. 5Minnesota Valley Engineering, Inc. 4Minnesota Medical Development, Inc. 3Minnesota Resuscitation Solutions, D.B.D Advancedcpr… 1Minnesota Medical Technologies 1The Minnesota Back Brace Co. 1