FDA applicant

Cantor & Nissel, Ltd.

Grand Junction, CO3 decisions2002–20040 recalls

FDA records 3 decisions for Cantor & Nissel, Ltd. (Grand Junction, CO) from 2002 to 2004: 3 510(k) clearances. Most are in product codes LPL (Lenses, Soft Contact, Daily Wear) and NIC (Lens, Contact, For Reading Discomfort). Its devices cite 5 predicates, 1 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 & Nissel, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cantor & Nissel, Ltd.’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 “Cantor”

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

Cantor & Silver, Ltd. 4

Cantor & Nissel, Ltd.

Which product codes does it file in?

Whose devices does it build on?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Cantor”