# K7, LLC

- Location (FDA's records): Chesterland, OH
- FDA decisions: 3 (2013–2014): 3 510(k) clearances
- Product codes: ODP (1), MNI (1), MAX (1)
- Predicates its devices cite: 26 (0 its own); citations of its devices by later devices: 1 (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
- K2m, Inc.: 6 (https://510kreport.com/company/k2m)
- Depuy Spine, Inc.: 3 (https://510kreport.com/company/depuy-spine)
- Eminent Spine: 2 (https://510kreport.com/company/eminent-spine)
- Ldr Spine USA: 2 (https://510kreport.com/company/ldr-spine-usa)
- Medtronic Sofamor Danek USA, Inc.: 2 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Depuyacromed: 2 (https://510kreport.com/company/depuyacromed)
- Stryker Spine: 2 (https://510kreport.com/company/stryker-spine)
- Sulzer Spine-Tech: 1 (https://510kreport.com/company/sulzer-spine-tech)

## Firms that cite its devices most
- Corentec Co., Ltd.: 1 (https://510kreport.com/company/corentec)

## Its most-cited devices
- K133126: K7 Lumbar Spacers (2013), cited by 1

## Recent decisions
- K133103: Aversion Pedicle Screw System (Jan 27, 2014)
- K133126: K7 Lumbar Spacers (Dec 9, 2013)
- K123388: K7C Spacer (Jan 4, 2013)

Source page: https://510kreport.com/company/k7