# Pilling Weck Surgical

- Location (FDA's records): Fort Washington, PA
- FDA decisions: 5 (1998–2000): 5 510(k) clearances
- Product codes: MWS (1), JOH (1), DXC (1), KNQ (1), JEK (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (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
- Passy-Muir, Inc.: 1 (https://510kreport.com/company/passy-muir)
- Rusch Intl.: 1 (https://510kreport.com/company/rusch-intl)

## Firms that cite its devices most
- Shikani Medical, LLC: 1 (https://510kreport.com/company/shikani-medical)

## Its most-cited devices
- K982128: Shikani-French Speaking Valve (1998), cited by 1

## Recent decisions
- K992476: Pilling Weck Surgical Heart Stabilizer Removable Pads (Sep 13, 2000)
- K992174: Pilling Weck Surgical Aortic Spoon-Jaw Clamp (Mar 23, 2000)
- K990935: Jackson Esophageal Dilator (May 17, 1999)
- K990561: Optical Forceps (May 14, 1999)
- K982128: Shikani-French Speaking Valve (Oct 23, 1998)

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