FDA applicant

Montrose Phototherapy Supply

Mchenry, IL2 decisions1981–19810 recalls

FDA records 2 decisions for Montrose Phototherapy Supply (Mchenry, IL) in 1981: 2 510(k) clearances. Most are in product codes LBI (Unit, Neonatal Phototherapy) and FOK (Pad, Neonatal Eye). 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 Montrose Phototherapy Supply’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Montrose Phototherapy Supply since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Montrose”

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

Montrose Intl., Corp. 1

Montrose Phototherapy Supply

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Montrose”