# Nemaris, Inc.

- Location (FDA's records): Washington, DC
- FDA decisions: 2 (2011–2014): 2 510(k) clearances
- Product codes: LLZ (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 15 (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
- Orthocrat, Ltd.: 2 (https://510kreport.com/company/orthocrat)

## Firms that cite its devices most
- S.M.A.I.O: 2 (https://510kreport.com/company/smaio)
- Medicrea International SA: 1 (https://510kreport.com/company/medicrea-international)
- Orthofix US, LLC: 1 (https://510kreport.com/company/orthofix-us)
- Alphatec Spine, Inc.: 1 (https://510kreport.com/company/alphatec-spine)
- Medtronic Sofamor Danek USA, Inc.: 1 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Onefit Medical: 1 (https://510kreport.com/company/onefit-medical)
- Abys Medical: 1 (https://510kreport.com/company/abys-medical)
- Ortho Kinematics, Inc.: 1 (https://510kreport.com/company/ortho-kinematics)

## Its most-cited devices
- K141669: Surgimap (2014), cited by 11
- K111019: Surgimap (TM) Spine (2011), cited by 4

## Recent decisions
- K141669: Surgimap (Sep 19, 2014)
- K111019: Surgimap (TM) Spine (Sep 30, 2011)

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