FDA applicant

Coopervision-Cilco

Bellevue, WA3 decisions1985–19880 recalls

FDA records 3 decisions for Coopervision-Cilco (Bellevue, WA) from 1985 to 1988: 2 510(k) clearances and 1 original PMA approval. Most are in product codes IYO (System, Imaging, Pulsed Echo, Ultrasonic) and KYB (Lens, Guide, Intraocular). 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 Coopervision-Cilco’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Coopervision-Cilco since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Coopervision-Cilco”

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

CooperVision, Inc. 106 Coopervision Surgical 3

Coopervision-Cilco

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Coopervision-Cilco”