FDA applicant

Bausch + Lomb Ireland Limited

Bridgewater1 decision2006–20060 recalls

FDA records 1 decision for Bausch + Lomb Ireland Limited (Bridgewater) in 2006: 1 original PMA approval. All are in product code MVF (System, Laser, Photodynamic Therapy). 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 Bausch + Lomb Ireland Limited’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bausch + Lomb Ireland Limited since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bausch + Lomb Ireland Limited by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Bausch”

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

Bausch & Lomb, Inc. 163 Bausch and Lomb, Incorporated 7 Bausch & Lomb Pharmaceutical, Inc. 6 Bausch Health Companies, Inc. 1 Bausch & Lomb Healthcare and Optics Worldwide 1 Bausch Health Americas Incorporated 1 Bausch Health 1 Bausch & Lomb Surgical, Inc. 1

Bausch + Lomb Ireland Limited

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bausch”