# Oral Osteodistraction, L.P.

- Location (FDA's records): Appollo Beach, FL
- FDA decisions: 3 (2003–2005): 3 510(k) clearances
- Product codes: MQN (3)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 2 (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
- KLS-Martin L.P.: 3 (https://510kreport.com/company/kls-martin)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)

## Firms that cite its devices most
- Mis - Implant Technologies, Ltd.: 1 (https://510kreport.com/company/mis-implant-technologies)

## Its most-cited devices
- K014001: Distraction Osteogenesis Rod Appliances, Models 1, 2, and 3 (2003), cited by 1
- K042278: Oral Osteodistraction Rod Appliance (Rod 5) (2005), cited by 1

## Recent decisions
- K042278: Oral Osteodistraction Rod Appliance (Rod 5) (Jan 28, 2005)
- K034045: Oral Osteodistraction Distraction Rod Appliances, Rod 4 (Mar 23, 2004)
- K014001: Distraction Osteogenesis Rod Appliances, Models 1, 2, and 3 (Feb 4, 2003)

Source page: https://510kreport.com/company/oral-osteodistraction
