# Weck

- Location (FDA's records): Durham, NC
- FDA decisions: 2 (2002–2003): 2 510(k) clearances
- Product codes: FZP (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 7 (0 its own)
- Recalls linked to its devices: 8 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Teleflex Medical: 3 (https://510kreport.com/company/teleflex-medical)
- Vesocclude Medical, LLC: 1 (https://510kreport.com/company/vesocclude-medical)
- A2 Medical Systems, LLC: 1 (https://510kreport.com/company/a2-medical-systems)
- AtriCure, Inc.: 1 (https://510kreport.com/company/atricure)
- Teleflexmedical, Inc.: 1 (https://510kreport.com/company/teleflexmedical)

## Its most-cited devices
- K030311: Hem-O-Lok XL Clip (2003), cited by 5
- K021808: Weck Hem-O-Lok Automatic Ligating Clip Applier (2002), cited by 2

## Recent decisions
- K030311: Hem-O-Lok XL Clip (Feb 26, 2003)
- K021808: Weck Hem-O-Lok Automatic Ligating Clip Applier (Aug 14, 2002)

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