FDA applicant

Physician Industries, Inc.

Salt Lake City, UT4 decisions1995–200433 recalls

FDA records 4 decisions for Physician Industries, Inc. (Salt Lake City, UT) from 1995 to 2004: 4 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and GXD (Generator, Lesion, Radiofrequency). Its devices cite 6 predicates, 0 of them its own earlier devices. 33 recalls are 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 Physician Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Physician Industries, Inc. since 2007.

Recalls per year

1in 2015

2007high 29 (2009) · low 0 (2007)2026

Class I Class II/III not classified

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

Planning a device like Physician Industries, Inc.’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 “Physician”

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

Physician Engineered Products, Inc. 8 Physician Technologies, Inc. 1 Physician Software Systems, LLC 1 Physician & Nurses Mfg. Corp. 1

Physician Industries, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Physician”