510(k) Report

FDA applicant

Medpro, Inc.

Mchenry, IL4 decisions1976–19770 recalls

FDA records 4 decisions for Medpro, Inc. (Mchenry, IL) from 1976 to 1977: 4 510(k) clearances. Most are in product codes IKY (Mattress, Flotation Therapy, Non-Powered) and FMP (Protector, Skin Pressure). 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, general hospital panel, where it files most

How often FDA has decided Medpro, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medpro, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medpro, 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?

  • IKYMattress, Flotation Therapy, Non-Powered2decisions
  • FMPProtector, Skin Pressure1decision
  • KICCushion, Flotation1decision

What has FDA decided for it lately?

  • K772062Neonatal Flotation SystemMedpro, Inc. · 1977
  • K771824Medpro Flotation SystemMedpro, Inc. · 1977
  • K760870Heel/Elbow Flotation CushionMedpro, Inc. · 1976
  • K760613Flotation Unit, ChairMedpro, Inc. · 1976

All 4 as Medpro, Inc. →

Other applicant names beginning “Medpro”

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

Medpro Safety Products, Inc. 3Medpro Technologies, Inc. 1