510(k) Report

FDA applicant

Medical Instrument Research Assoc., Inc.

Mchenry, IL4 decisions1976–19790 recalls

FDA records 4 decisions for Medical Instrument Research Assoc., Inc. (Mchenry, IL) from 1976 to 1979: 4 510(k) clearances. Most are in product codes HOZ (Sponge, Ophthalmic) and HQJ (Implant, Absorbable, (Scleral Buckling Methods)). 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 Medical Instrument Research Assoc., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medical Instrument Research Assoc., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medical Instrument Research Assoc., 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?

  • HOZSponge, Ophthalmic1decision
  • HQJImplant, Absorbable, (Scleral Buckling Methods)1decision
  • HKICamera, Ophthalmic, Ac-Powered1decision
  • HLIOphthalmoscope, Ac-Powered1decision

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.

  • K780987Soft Silicone Elastomer Sponge ExplantMedical Instrument Research Assoc., Inc. · 19781cites it

What has FDA decided for it lately?

  • K791510Blue Field Entoptoscope BFE100Medical Instrument Research Assoc., Inc. · 1979
  • K780987Soft Silicone Elastomer Sponge ExplantMedical Instrument Research Assoc., Inc. · 1978
  • K770888Pomerantzeff Equator Plus CameraMedical Instrument Research Assoc., Inc. · 1977
  • K760550Implant, Silicone and TantalumMedical Instrument Research Assoc., Inc. · 1976

All 4 as Medical Instrument Research Assoc., Inc. →