510(k) Report

FDA applicant

Prosthetic Soft Lens Corp.

Englewood, CO1 decision1999–19990 recalls

FDA records 1 decision for Prosthetic Soft Lens Corp. (Englewood, CO) in 1999: 1 510(k) clearance. All are in product code LPL (Lenses, Soft Contact, Daily Wear). Its devices cite 3 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, ophthalmic panel, where it files most

How often FDA has decided Prosthetic Soft Lens Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Prosthetic Soft Lens Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Which product codes does it file in?

  • LPLLenses, Soft Contact, Daily Wear1decision

Whose devices does it build on?

Its devices cite 3 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.

  • K992950Custom Prosthetic (Hefilcon a) Soft LensProsthetic Soft Lens Corp. · 19992cite it

What has FDA decided for it lately?

  • K992950Custom Prosthetic (Hefilcon a) Soft LensProsthetic Soft Lens Corp. · 1999

The one decision as Prosthetic Soft Lens Corp. →