FDA applicant

Pilling Weck, Inc.

Research Triangle Park, NC6 decisions1994–19990 recalls

FDA records 6 decisions for Pilling Weck, Inc. (Research Triangle Park, NC) from 1994 to 1999: 6 510(k) clearances. Most are in product codes GDT (Staple, Removable (Skin)) and FZP (Clip, Implantable). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Pilling Weck, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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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 Group 5 Pilling Weck Surgical 5 Pilling Medical S.A. 1

Pilling Weck, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Pilling”