FDA applicant

Pilling Weck Surgical

Fort Washington, PA5 decisions1998–20000 recalls

FDA records 5 decisions for Pilling Weck Surgical (Fort Washington, PA) from 1998 to 2000: 5 510(k) clearances. Most are in product codes MWS (Stabilizer, Heart) and JOH (Tube Tracheostomy And Tube Cuff). Its devices cite 2 predicates, 0 of them its own earlier devices. 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Pilling Weck Surgical since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Pilling Weck Surgical’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Pilling”

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

Pilling Co. 40 Pilling Weck, Inc. 6 Pilling Weck Group 5 Pilling Medical S.A. 1

Pilling Weck Surgical

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?

Other applicant names beginning “Pilling”