# Ebi,Llc D/B/A Biomet Trauma

- Location (FDA's records): Parsippany, NJ
- FDA decisions: 1 (2009–2009): 1 510(k) clearance
- Product codes: HRS (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 5 (0 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
- TriMed, Inc.: 1 (https://510kreport.com/company/trimed)
- Biomet Orthopedics, Inc.: 1 (https://510kreport.com/company/biomet-orthopedics)
- Ebi, L.P.: 1 (https://510kreport.com/company/ebi)

## Firms that cite its devices most
- Life Spine, Inc.: 1 (https://510kreport.com/company/life-spine)
- Nextremity Solutions, Inc.: 1 (https://510kreport.com/company/nextremity-solutions)
- I.T.S. GmbH: 1 (https://510kreport.com/company/its)
- Biomet, Inc.: 1 (https://510kreport.com/company/biomet)
- Ortho Solutions Limited: 1 (https://510kreport.com/company/ortho-solutions)

## Its most-cited devices
- K092670: Biodrive Micro Screw System (2009), cited by 5

## Recent decisions
- K092670: Biodrive Micro Screw System (Nov 19, 2009)

Source page: https://510kreport.com/company/ebi-d-b-a-biomet-trauma