# Denver Biomaterials, Inc.

- Location (FDA's records): Evergreen, CO
- FDA decisions: 4 (1996–1998): 4 510(k) clearances
- Product codes: KPM (2), KDD (1), DWM (1)
- Predicates its devices cite: 4 (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
- Codman & Shurtleff, Inc.: 1 (https://510kreport.com/company/codman-shurtleff)
- Denver Biomedicals, Inc.: 1 (https://510kreport.com/company/denver-biomedicals)
- Endovations: 1 (https://510kreport.com/company/endovations)
- Tri-Med Specialties, Inc.: 1 (https://510kreport.com/company/tri-med-specialties)

## Firms that cite its devices most
- Bard Access Systems, Inc.: 1 (https://510kreport.com/company/bard-access-systems)

## Its most-cited devices
- K971753: Denver Pleurx Pleural Catheter Kit, Catalog NO. 50-7000, Denver Pleurx Home Drainage Kit, Catalog NO. 50-7500 (1997), cited by 1

## Recent decisions
- K973129: Denver Ascites Shunts, Denver Ascites Shunt Percutaneous Access Kits (Mar 17, 1998)
- K971753: Denver Pleurx Pleural Catheter Kit, Catalog NO. 50-7000, Denver Pleurx Home Drainage Kit, Catalog NO. 50-7500 (Jun 27, 1997)
- K962814: Denver Pleural Effusion Shunt with External Pump Chamber (Apr 14, 1997)
- K960456: Denver Paracentesis Needle (60-1200) Denver Paracentesis Needle with Drainage Line (60-1100) Denver Paracentesis Tray (Apr 1, 1996)

Source page: https://510kreport.com/company/denver-biomaterials