FDA applicant

Pharmacia Iovision, Inc.

Peapack, NJ1 decision1997–19970 recalls

FDA records 1 decision for Pharmacia Iovision, Inc. (Peapack, NJ) in 1997: 1 510(k) clearance. All are in product code KYF (Implant, Eye Valve). 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 Pharmacia Iovision, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pharmacia Iovision, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Pharmacia”

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

Pharmacia, Inc. 130 Pharmacia Deltec, Inc. 43 Pharmacia & Upjohn Co. 18 Pharmacia Diagnostics, Inc. 10 Pharmacia Deutschland GmbH 10 Pharmacia Eni Diagnostics, Inc. 2 Pharmacia Hepar, Inc. 1 Pharmacia Fine Chemicals 1

Pharmacia Iovision, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Pharmacia”