# Innerspace, Inc.

- Location (FDA's records): Santa Ana, CA
- FDA decisions: 8 (2001–2012): 8 510(k) clearances
- Product codes: GWM (7), HCA (1)
- Predicates its devices cite: 10 (7 its own); citations of its devices by later devices: 8 (7 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
- Integra Neurosciences: 2 (https://510kreport.com/company/integra-neurosciences)
- Camino Neurocare, Inc.: 1 (https://510kreport.com/company/camino-neurocare)

## Firms that cite its devices most
- Innerspace Neuro Solutions, Inc.: 1 (https://510kreport.com/company/innerspace-neuro-solutions)

## Its most-cited devices
- K013705: Act Iii Ventricular Catheter (2002), cited by 2
- K041838: MPS (or MPS-T) (2005), cited by 1
- K072379: MPS Oxiport and MPS Oxiport Plus (2008), cited by 1
- K013005: Act 11 MP Ventricular Catheter (2002), cited by 1
- K083378: Synergy (2009), cited by 1
- K010422: Act II Icp Monitoring System and Ventricular Catheter (2001), cited by 1

## Recent decisions
- K113088: Hummingbird Subdural H900DS (Drainage and Icp), Hummingbird Subdural- H800S (Icp Only) (May 2, 2012)
- K083378: Synergy (Sep 29, 2009)
- K072379: MPS Oxiport and MPS Oxiport Plus (Apr 29, 2008)
- K041838: MPS (or MPS-T) (Mar 1, 2005)
- K013705: Act Iii Ventricular Catheter (Sep 9, 2002)
- K013005: Act 11 MP Ventricular Catheter (Mar 8, 2002)
- K010422: Act II Icp Monitoring System and Ventricular Catheter (Jun 28, 2001)
- K003905: Acti-Icp Monitoring System (Jun 15, 2001)

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