FDA applicant

Pfizer Laser Systems

Irvine, CA32 decisions1988–19930 recalls

FDA records 32 decisions for Pfizer Laser Systems (Irvine, CA) from 1988 to 1993: 32 510(k) clearances. Most are in product codes GEX (Powered Laser Surgical Instrument) and HQF (Laser, Ophthalmic). 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, general and plastic surgery panel, where it files most

How often FDA has decided Pfizer Laser Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pfizer Laser Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Pfizer”

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

Pfizer, Inc. 39 Pfizer Medical Systems, Inc. 12 Pfizer Hospital Products Group, Inc. 8 Pfizer Pharmaceuticals 6

Pfizer Laser Systems

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 “Pfizer”