FDA applicant

Phoenix Laser Systems, Inc.

St.Petersburg, FL1 decision1990–19900 recalls

FDA records 1 decision for Phoenix Laser Systems, Inc. (St.Petersburg, FL) in 1990: 1 510(k) clearance. All are in product code LXS (Laser, Neodymium:Yag, Ophthalmic For Posterior…). 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 Phoenix Laser Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Phoenix Laser Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Phoenix Laser Systems, 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 “Phoenix”

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

Phoenix Diagnostics, Inc. 21 Phoenix Biomedical Corp. 13 Phoenix Medical Technology, Inc. 11 Phoenix Glove Co. 6 Phoenix Dental, Inc. 5 Phoenix Bioengineering, Inc. 3 Phoenix Medical Devices, LLC 2 Phoenix Innovative Healthcare Manufacturers Pvt., Ltd. 2 Phoenix Biotech Corp. 2 Phoenix Imaging 2 Phoenix Surgical Products, Inc. 1 Phoenix Management, Inc. 1

Phoenix Laser Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Phoenix”