# Orthocor Medical

- Location (FDA's records): Mccordsville, IN
- FDA decisions: 3 (2009–2013): 3 510(k) clearances
- Product codes: ILX (3)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 4 (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
- Ivivi Technologies, Inc.: 2 (https://510kreport.com/company/ivivi-technologies)

## Firms that cite its devices most
- Caerus Corporation: 2 (https://510kreport.com/company/caerus)
- Bioelectronics Corporation: 1 (https://510kreport.com/company/bioelectronics)

## Its most-cited devices
- K092044: Orthocor Knee System, Median, Large, X-Large (2009), cited by 2
- K121702: Orthocor Active Device Orthocor General Use Active Device (2013), cited by 1
- K091996: Orthocor Knee System Basic (2009), cited by 1

## Recent decisions
- K121702: Orthocor Active Device Orthocor General Use Active Device (May 6, 2013)
- K092044: Orthocor Knee System, Median, Large, X-Large (Dec 18, 2009)
- K091996: Orthocor Knee System Basic (Dec 15, 2009)

Source page: https://510kreport.com/company/orthocor-medical