FDA applicant

Ocular Pharmaceuticals, Inc.

New York, NY1 decision1988–19880 recalls

FDA records 1 decision for Ocular Pharmaceuticals, Inc. (New York, NY) in 1988: 1 510(k) clearance. All are in product code LPN (Accessories, Soft Lens Products). 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 Ocular Pharmaceuticals, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ocular Pharmaceuticals, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ocular Pharmaceuticals, 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 “Ocular”

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

Ocular Instruments, Inc. 50 Ocular Sciences Puerto Rico, Inc. 7 Ocular Therapeutix, Inc. 2 Ocular Sciences 2 Ocular Innovations, Inc. 2 Ocular Blood Flow Laboratories, Inc. 2 Ocular Concepts, LLC 1 Ocular Systems, Inc. 1

Ocular Pharmaceuticals, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ocular”