510(k) Report

FDA applicant

Coherent Radiation Laboratories

Walker, MI3 decisions1982–19830 recalls

FDA records 3 decisions for Coherent Radiation Laboratories (Walker, MI) from 1982 to 1983: 3 510(k) clearances. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Coherent Radiation Laboratories’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Coherent Radiation Laboratories since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Coherent Radiation Laboratories by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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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.

  • K837235Model 920 Argon Laser SystemCoherent Radiation Laboratories · 19831cites it

What has FDA decided for it lately?

  • K837235Model 920 Argon Laser SystemCoherent Radiation Laboratories · 1983
  • K837125System 900 Two Room Remote FibersCoherent Radiation Laboratories · 1983
  • K827383Model 900 Photocoagulator with Green-Only OptionsCoherent Radiation Laboratories · 1982

All 3 as Coherent Radiation Laboratories →

Other applicant names beginning “Coherent”

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

Coherent Medical Group 27Coherent Medical Division 7Coherent Systems, Inc. 3Coherent Medical Lasers 2Coherent Star 2