# Hogan Lovells US LLP

- Location (FDA's records): Philedelphia, PA
- FDA decisions: 3 (2012–2014): 3 510(k) clearances
- Product codes: NKB (1), OWI (1), GEX (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 3 (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
- Aesculap Implant Systems, LLC: 1 (https://510kreport.com/company/aesculap-implant-systems)
- Medtronic Sofamor Danek USA, Inc.: 1 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Zimmer Spine, Inc.: 1 (https://510kreport.com/company/zimmer-spine)
- Implanet, S.A.: 1 (https://510kreport.com/company/implanet)

## Firms that cite its devices most
- Implanet, S.A.: 3 (https://510kreport.com/company/implanet)

## Its most-cited devices
- K120564: Calypso System (2012), cited by 2
- K132287: Jazz System (2013), cited by 1

## Recent decisions
- K122358: Noveon (Mar 11, 2014)
- K132287: Jazz System (Sep 25, 2013)
- K120564: Calypso System (Jul 16, 2012)

Source page: https://510kreport.com/company/hogan-lovells-us