# Vertis Neuroscience, Inc.

- Location (FDA's records): Seattle, WA
- FDA decisions: 2 (2001–2002): 2 510(k) clearances
- Product codes: NHI (2)
- Predicates its devices cite: 12 (1 its own); citations of its devices by later devices: 2 (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
- Empi: 4 (https://510kreport.com/company/empi)
- Rehabilicare, Inc.: 2 (https://510kreport.com/company/rehabilicare)
- Medtronic Vascular: 2 (https://510kreport.com/company/medtronic-vascular)
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)
- Medelec, Inc. D.B.A. Teca Corp.: 1 (https://510kreport.com/company/medelec-dba-teca)
- Dantec Medical, Inc.: 1 (https://510kreport.com/company/dantec-medical)

## Firms that cite its devices most
- Biowave Corporation: 1 (https://510kreport.com/company/biowave)

## Its most-cited devices
- K011702: Vertis PNT Control Unit, Vertis PNT Safeguide Kids, Models CU100, Sgxxx (2001), cited by 1
- K022241: Vertis PNT Control Unit, Model CU 100; Vertis PNT Safeguide-Cervical, Model SG 102-XXX (2002), cited by 1

## Recent decisions
- K022241: Vertis PNT Control Unit, Model CU 100; Vertis PNT Safeguide-Cervical, Model SG 102-XXX (Sep 11, 2002)
- K011702: Vertis PNT Control Unit, Vertis PNT Safeguide Kids, Models CU100, Sgxxx (Dec 21, 2001)

Source page: https://510kreport.com/company/vertis-neuroscience