# Whiteside Biomechanics, Inc.

- Location (FDA's records): Creve Coeur, MO
- FDA decisions: 13 (1996–2004): 13 510(k) clearances
- Product codes: LZO (3), LPH (3), NDD (1), HWC (1), HRY (1), KWY (1), LWJ (1), JDQ (1), KWQ (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 3 (1 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
- Intermedics Orthopedics: 1 (https://510kreport.com/company/intermedics-orthopedics)
- Biomechanic, Inc.: 1 (https://510kreport.com/company/biomechanic)
- Corin USA: 1 (https://510kreport.com/company/corin-usa)

## Firms that cite its devices most
- Intelligent Implant Systems, LLC: 1 (https://510kreport.com/company/intelligent-implant-systems)
- United Orthopedic Corporation: 1 (https://510kreport.com/company/united-orthopedic)

## Its most-cited devices
- K961157: Whiteside Biomechanics Cancellous Bone Screw (1996), cited by 1
- K981238: Bipolar Femoral Head (1998), cited by 1
- K964616: Quatroloc Plasma Sprayed Femoral Component (1997), cited by 1

## Recent decisions
- K033313: Quatro M Femoral Component (Jul 28, 2004)
- K012800: Symmetric Unicompartmental Knee System (May 3, 2002)
- K003618: Whiteside Biomechanics Low Profile Stainless Steel Cable System, Model Bio-1-1014 (May 23, 2001)
- K993903: Whiteside Biomechanics Titanium Low-Profile Cable, Model Bio-1-1013 (Feb 14, 2000)
- K991678: Whiteside Biomechanics Spinal System (Aug 12, 1999)
- K981238: Bipolar Femoral Head (Aug 21, 1998)
- K973261: Whiteside Biomechanics, Inc. Ceramic Unipolar Femoral Head (Nov 24, 1997)
- K964616: Quatroloc Plasma Sprayed Femoral Component (Aug 7, 1997)

Source page: https://510kreport.com/company/whiteside-biomechanics