# Pilling Weck, Inc.

- Location (FDA's records): Research Triangle Park, NC
- FDA decisions: 6 (1994–1999): 6 510(k) clearances
- Product codes: GDT (1), FZP (1), EOQ (1), GCJ (1), GEI (1), DWS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K990547: Pilling Weck Surgical Y Stent Forceps (Apr 27, 1999)
- K974250: Versastat Multipolar Scissors and Cables (Feb 11, 1998)
- K962771: Burke Congenital Thoracoscopy Instruments (Nov 19, 1996)
- K945520: Hemoclip Ecosystem (Jan 27, 1995)
- K944552: Pilling Weck M-20 Disposable Automatic Hemoclip (Nov 7, 1994)
- K943719: Visistat Stapler (Aug 24, 1994)

Source page: https://510kreport.com/company/pilling-weck