FDA applicant

Cantor & Silver, Ltd.

Grand Junction, CO4 decisions1998–20000 recalls

FDA records 4 decisions for Cantor & Silver, Ltd. (Grand Junction, CO) from 1998 to 2000: 4 510(k) clearances. Most are in product codes LPL (Lenses, Soft Contact, Daily Wear) and NCZ (Lens, Contact, For Color Vision Deficiency). Its devices cite 1 predicate, 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 Cantor & Silver, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cantor & Silver, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Cantor”

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

Cantor & Nissel, Ltd. 3

Cantor & Silver, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Cantor”