FDA applicant

Bausch & Lomb Pharmaceutical, Inc.

Clearwater, FL6 decisions1988–19900 recalls

FDA records 6 decisions for Bausch & Lomb Pharmaceutical, Inc. (Clearwater, FL) from 1988 to 1990: 6 510(k) clearances. Most are in product codes MOE (Collagen Corneal Shield) and HQJ (Implant, Absorbable, (Scleral Buckling Methods)). 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 Pharmaceutical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bausch & Lomb Pharmaceutical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bausch & Lomb Pharmaceutical, 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 “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 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 1

Bausch & Lomb Pharmaceutical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bausch”