# Optimotion Implants, LLC

- Location (FDA's records): Orlando, FL
- FDA decisions: 3 (2020–2024): 3 510(k) clearances
- Product codes: MBH (3)
- 510(k) review time since 2016: median 83 days, against 84 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 1 (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
- Stryker Orthopaedics: 2 (https://510kreport.com/company/stryker-orthopaedics)
- Consensus Orthopedics, Inc.: 1 (https://510kreport.com/company/consensus-orthopedics)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)

## Its most-cited devices
- K191084: The Optimotion Blue Total Knee System (2020), cited by 1

## Recent decisions
- K240938: The Optimotion™ Blue Plus Knee System (Jun 27, 2024)
- K220049: Optimotion Implants Porous Metal-Backed Patella (Mar 14, 2022)
- K191084: The Optimotion Blue Total Knee System (Apr 7, 2020)

Source page: https://510kreport.com/company/optimotion-implants