FDA applicant

Phoenix Medical Technology, Inc.

Andrews, SC11 decisions1986–20000 recalls

FDA records 11 decisions for Phoenix Medical Technology, Inc. (Andrews, SC) from 1986 to 2000: 11 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and LYZ (Vinyl Patient Examination Glove). 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 hospital panel, where it files most

How often FDA has decided Phoenix Medical Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Phoenix Medical Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Phoenix Medical Technology, 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 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 U.V.A., Ltd. 1

Phoenix Medical Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Phoenix”