FDA applicant

Professional Instruments Co.

Houston, TX3 decisions1981–19870 recalls

FDA records 3 decisions for Professional Instruments Co. (Houston, TX) from 1981 to 1987: 3 510(k) clearances. Most are in product codes BXN (Stimulator, Nerve, Battery-Powered) and GXY (Electrode, Cutaneous). 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, anesthesiology panel, where it files most

How often FDA has decided Professional Instruments Co.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Professional Instruments Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Professional”

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

Professional Medical Services 19 Professional Medical Products, Inc. 9 Professional Latex Sdn Bhd 3 Professional Positioners, Inc. 3 Professional Tape Co., Inc. 2 Professional Services For Surgeons, Ltd. 2 Professional Dental Mfg., Inc. 2 Professional Technologies Corp. 2 Professional Supplies, Inc. 2 Professional Disposables International, Inc. 1 Professional Medical Systems 1 Professional Pharmacy West, Inc. 1

Professional Instruments Co.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Professional”