510(k) Report

FDA applicant

Skylit Medical

La Jolla, CA1 decision2017–20170 recalls

FDA records 1 decision for Skylit Medical (La Jolla, CA) in 2017: 1 510(k) clearance. All are in product code FTC (Light, Ultraviolet, Dermatological). Its devices cite 4 predicates, 0 of them its own earlier devices. 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 and plastic surgery panel, where it files most

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

FDA decisions per year

1in 2017

2017: 1
2017high 1 (2017) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Skylit Medical by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Skylit Medical’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

Which product codes does it file in?

  • FTCLight, Ultraviolet, Dermatological1decision

Whose devices does it build on?

Its devices cite 4 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K170489Skylit Phototherapy SystemSkylit Medical · 20172cite it

What has FDA decided for it lately?

  • K170489Skylit Phototherapy SystemSkylit Medical · 2017

The one decision as Skylit Medical →