510(k) Report

FDA applicant

Innomed Corp.

Brea, CA3 decisions1982–19870 recalls

FDA records 3 decisions for Innomed Corp. (Brea, CA) from 1982 to 1987: 3 510(k) clearances. Most are in product codes HMR (Marker, Ocular) and LJL (Detectors And Removers, Lice, (Including Combs)). 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 Innomed Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Innomed Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Innomed Corp. 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?

  • HMRMarker, Ocular1decision
  • LJLDetectors And Removers, Lice, (Including Combs)1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K822574Innomed PD-1 KitInnomed Corp. · 19822cite it

What has FDA decided for it lately?

  • K872747Laser Centering DeviceInnomed Corp. · 1987
  • K822574Innomed PD-1 KitInnomed Corp. · 1982
  • K827796Innoscan Examination LightInnomed Corp. · 1982

All 3 as Innomed Corp. →

Other applicant names beginning “Innomed”

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

Innomed Technologies 3Innomed Technologies, Inc./Respcare, Inc. 2Innomed Healthscience, Inc. 1