510(k) Report

FDA applicant

Professional Technologies Corp.

Redding, CA2 decisions1989–19920 recalls

FDA records 2 decisions for Professional Technologies Corp. (Redding, CA) from 1989 to 1992: 2 510(k) clearances. Most are in product codes HKX (Tonometer, Ac-Powered) and KLE (Agent, Tooth Bonding, Resin). 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 Professional Technologies Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Professional Technologies Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Professional Technologies Corp. 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.