# Edward Weck, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 140 (1976–1992): 140 510(k) clearances
- Product codes: HNR (14), GEI (8), FZP (7), FZT (5), GEN (5), GDJ (5), KAE (4), GDO (4), GAD (4), HND (4), HNQ (4), GDG (3)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (0 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Vesocclude Medical, LLC: 4 (https://510kreport.com/company/vesocclude-medical)
- Design Standards Corp.: 1 (https://510kreport.com/company/design-standards)
- Teleflex Medical: 1 (https://510kreport.com/company/teleflex-medical)
- Scanlan Intl., Inc.: 1 (https://510kreport.com/company/scanlan-intl)
- Vitalitec Int'L., Inc.: 1 (https://510kreport.com/company/vitalitec-int-l)
- Eisner USA, Inc.: 1 (https://510kreport.com/company/eisner-usa)

## Its most-cited devices
- K800079: Hemoclip Surgical Occluding Clip (1980), cited by 2
- K841547: Hemoclip Ligating Clips Med/SML (1984), cited by 2
- K902108: Hem-O-Lok (TM) (1990), cited by 1
- K841549: Hemoclip Automatic Clips Medium (1984), cited by 1
- K790413: Heifetz Aneurysm Clip, LMM Blade (1979), cited by 1
- K851251: Auto/Manual Titanium Hemoclip Ligating Clip 527200 (1985), cited by 1

## Recent decisions
- K915378: Weck Trocar (Jun 29, 1992)
- K914690: LM15(TM), Catalog Number - 523821 (Mar 23, 1992)
- K911915: Hemoclip II (Jan 9, 1992)
- K914470: Pneumo-Seal (TM) (Nov 29, 1991)
- K911272: Endoscopic Needlholder Cat. Number 114705 (Jul 2, 1991)
- K902108: Hem-O-Lok (TM) (Aug 6, 1990)
- K902232: Weck Electrosurgical Generator #174200 (Aug 2, 1990)
- K897045: Bowie-Dick Test Card Catalog Number 008018 (Feb 15, 1990)

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