FDA applicant

Solar Electronics

Mchenry, IL1 decision1981–19810 recalls

FDA records 1 decision for Solar Electronics (Mchenry, IL) in 1981: 1 510(k) clearance. All are in product code KNG (Monitor, Ultrasonic, Fetal). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Solar Electronics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Solar Electronics since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Solar Electronics’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Solar”

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

Solar Dental Co., Inc. 6 Solar Laboratories, Inc. 5 Solar Aid Corp. 1 Solar Mobilityllc 1 Solar Technologies Corp. 1 Solar Pacific 1 Solar LS Cjsc 1 Solar Sunglasses Corp. 1

Solar Electronics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Solar”