FDA applicant

Pilling Co.

Fort Washington, PA40 decisions1976–20000 recalls

FDA records 40 decisions for Pilling Co. (Fort Washington, PA) from 1976 to 2000: 40 510(k) clearances. Most are in product codes DWS (Instruments, Surgical, Cardiovascular) and FCW (Light Source, Fiberoptic, Routine). No recall is linked to its devices.

FDA’s records also spell it “Pilling”.

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

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

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

FDA decisions per year

No FDA decision for Pilling Co. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pilling Co.’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 “Pilling”

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

Pilling Weck, Inc. 6 Pilling Weck Group 5 Pilling Weck Surgical 5 Pilling Medical S.A. 1

Pilling Co.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Pilling”