# Conventus Orthopaedics, Inc.

- Location (FDA's records): Maple Grove, MN
- FDA decisions: 6 (2013–2021): 6 510(k) clearances
- Names in FDA's records: Conventus Orthopaedics, Inc. (3); Conventus Orthopaedics (2); Conventus Orthopaedics, LLC (1)
- Product codes: HRS (4), HSB (1), JDS (1)
- Predicates its devices cite: 15 (7 its own); citations of its devices by later devices: 9 (7 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Synthes (Usa): 4 (https://510kreport.com/company/synthes-usa)
- Sonoma Orthopedic Products, Inc.: 1 (https://510kreport.com/company/sonoma-orthopedic-products)
- Wrightmedicaltechnologyinc: 1 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Intrafuse, LLC: 1 (https://510kreport.com/company/intrafuse)
- Depuy Ace Medical Co.: 1 (https://510kreport.com/company/depuy-ace-medical)

## Firms that cite its devices most
- Flower Orthopedics Corporation Dba Conventus Flower: 2 (https://510kreport.com/company/flower-orthopedics-dba-conventus-flower)

## Its most-cited devices
- K102689: Conventus Orthopaedics Fracture Fixation System (2013), cited by 4
- K131552: Conventus DRS (2014), cited by 2
- K202858: Flex-ThreadTM Distal Fibula Intramedullary Nail System (2021), cited by 2
- K151379: Conventus PRS System (2015), cited by 1

## Recent decisions
- K202858: Flex-ThreadTM Distal Fibula Intramedullary Nail System (Jan 22, 2021)
- K161048: Conventus Orthopaedics Ulna Fixation System (Jul 26, 2016)
- K151379: Conventus PRS System (Aug 13, 2015)
- K141737: Conventus PHS System (Apr 8, 2015)
- K131552: Conventus DRS (Feb 12, 2014)
- K102689: Conventus Orthopaedics Fracture Fixation System (Jan 17, 2013)

Source page: https://510kreport.com/company/conventus-orthopaedics