FDA applicant

Percutaneous Technologies

Walnut, CA3 decisions1990–19970 recalls

FDA records 3 decisions for Percutaneous Technologies (Walnut, CA) from 1990 to 1997: 3 510(k) clearances. Most are in product codes HEX (Colposcope (And Colpomicroscope)) and DXC (Clamp, Vascular). No recall is linked to its devices.

FDA’s records also spell it “Percutaneous Technologies, Inc.”.

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

FIG. A — Illustration, obstetrics and gynecology panel, where it files most

How often FDA has decided Percutaneous Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Percutaneous Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Percutaneous Technologies’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 “Percutaneous”

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

Percutaneous Systems, Inc. 11

Percutaneous Technologies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Percutaneous”