FDA applicant

Phoenix Biomedical Corp.

Valley Forge, PA13 decisions1996–20040 recalls

FDA records 13 decisions for Phoenix Biomedical Corp. (Valley Forge, PA) from 1996 to 2004: 13 510(k) clearances. Most are in product codes JXG (Shunt, Central Nervous System And Components) and GAS (Suture, Nonabsorbable, Synthetic, Polyester). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Phoenix Biomedical”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, neurology panel, where it files most

How often FDA has decided Phoenix Biomedical Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Phoenix Biomedical Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Phoenix Biomedical Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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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 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 U.V.A., Ltd. 1

Phoenix Biomedical Corp.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Phoenix”