510(k) Report

FDA applicant

Precision Medical Instruments, Inc.

Mchenry, IL4 decisions1979–19850 recalls

FDA records 4 decisions for Precision Medical Instruments, Inc. (Mchenry, IL) from 1979 to 1985: 4 510(k) clearances. Most are in product codes HQE (Instrument, Vitreous Aspiration And Cutting…) and HMX (Cannula, Ophthalmic). 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, ophthalmic panel, where it files most

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

FDA decisions per year

No FDA decision for Precision Medical Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Precision Medical Instruments, 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?

  • HQEInstrument, Vitreous Aspiration And Cutting, Ac-Powered2decisions
  • HMXCannula, Ophthalmic1decision

What has FDA decided for it lately?

  • K852758Infusion CannulamPrecision Medical Instruments, Inc. · 1985
  • K832560Aspirating Handle W/Backflushing CapabPrecision Medical Instruments, Inc. · 1984
  • K830037Extension Handle for Acutome ProbePrecision Medical Instruments, Inc. · 1983
  • K791212Vitrectomy Integrating Tray Ocutome/FragPrecision Medical Instruments, Inc. · 1979

All 4 as Precision Medical Instruments, Inc. →