FDA applicant

Bausch & Lomb Healthcare and Optics Worldwide

Tampa, FL1 decision1995–19950 recalls

FDA records 1 decision for Bausch & Lomb Healthcare and Optics Worldwide (Tampa, FL) in 1995: 1 510(k) clearance. All are in product code MOE (Collagen Corneal Shield). 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 Healthcare and Optics Worldwide’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bausch & Lomb Healthcare and Optics Worldwide since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bausch & Lomb Healthcare and Optics Worldwide 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 Health Americas Incorporated 1 Bausch Health 1 Bausch & Lomb Surgical, Inc. 1 Bausch + Lomb Ireland Limited 1

Bausch & Lomb Healthcare and Optics Worldwide

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bausch”