# Pilling Weck Group

- Location (FDA's records): Jeffrey, NH
- FDA decisions: 5 (1996–1997): 5 510(k) clearances
- Product codes: GCJ (3), OCZ (1), HET (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)

## Firms that cite its devices most
- Advanced Medical Innovations, Inc.: 1 (https://510kreport.com/company/advanced-medical-innovations)
- Xomed, Inc.: 1 (https://510kreport.com/company/xomed)
- Medisiss: 1 (https://510kreport.com/company/medisiss)

## Its most-cited devices
- K964450: Secondary Trocar and Sleeve with Insufflation Port (1997), cited by 2
- K965176: Pilling Weck 2 Piece Take-Apart Instruments (1997), cited by 1

## Recent decisions
- K971334: Pilling Weck Secondary Flexible Sleeve with Trocar (Jun 11, 1997)
- K965176: Pilling Weck 2 Piece Take-Apart Instruments (Mar 4, 1997)
- K964450: Secondary Trocar and Sleeve with Insufflation Port (Jan 10, 1997)
- K964123: Reusable Trocar with Sleeve (Common) (Dec 12, 1996)
- K963815: Reusable Trocar with Sleeve (Common) (Nov 5, 1996)

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