# Biologically Oriented Prostheses

- Location (FDA's records): Port Huron, MI
- FDA decisions: 9 (1995–2000): 9 510(k) clearances
- Product codes: LZO (3), LPH (2), JDC (1), KYI (1), JDS (1), JDI (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Dow Corning Wright: 1 (https://510kreport.com/company/dow-corning-wright)

## Firms that cite its devices most
- I.T.S. Implantat-Technologie-Systeme GmbH: 1 (https://510kreport.com/company/its-implantat-technologie-systeme)
- Signal Medical Corp.: 1 (https://510kreport.com/company/signal-medical)
- Ascension Orthopedics, Inc.: 1 (https://510kreport.com/company/ascension-orthopedics)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)
- Biopro, Inc.: 1 (https://510kreport.com/company/biopro)

## Its most-cited devices
- K962769: Horizon Hip System (1996), cited by 2
- K955916: Townley Total Elbow System (1996), cited by 1
- K964472: Riopro Cobalt Trapeziometarcarpal Resurfacing Component (1997), cited by 1
- K002325: Wujin #3 Tibial Nail (2000), cited by 1

## Recent decisions
- K002325: Wujin #3 Tibial Nail (Oct 30, 2000)
- K992144: Biopro Rimmed Acetabular Compoment (Sep 22, 1999)
- K964472: Riopro Cobalt Trapeziometarcarpal Resurfacing Component (Feb 3, 1997)
- K962769: Horizon Hip System (Oct 3, 1996)
- K955916: Townley Total Elbow System (Aug 8, 1996)
- K954768: Biopro Hemi-Endo Modular Ceramic Head (Jan 18, 1996)
- K952731: Townley All Poly Acetabular Cup (Dec 28, 1995)
- K953045: Biopro Hemi-Endo Modular Ceramic Head (Sep 27, 1995)

Source page: https://510kreport.com/company/biologically-oriented-prostheses