# Parallax Medical, Inc.

- Location (FDA's records): Scotts Valley, CA
- FDA decisions: 6 (1999–2003): 6 510(k) clearances
- Product codes: MYU (3), KNW (2), GXP (1)
- Predicates its devices cite: 5 (3 its own); citations of its devices by later devices: 8 (3 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
- Dentsply Intl.: 2 (https://510kreport.com/company/dentsply-intl)

## Firms that cite its devices most
- Stryker Corp.: 2 (https://510kreport.com/company/stryker)
- Regulatory Specialists, Inc.: 1 (https://510kreport.com/company/regulatory-specialists)
- Pneumrx, Inc.: 1 (https://510kreport.com/company/pneumrx)
- Vidacare Corporation: 1 (https://510kreport.com/company/vidacare)

## Its most-cited devices
- K022169: Clearview Plus Bone and Vertebral Body Biopsy Needles (2002), cited by 4
- K011206: Parallax Bone and Vertebral Body Biopsy and Infusion Needles (2001), cited by 2
- K023445: Tracers Bone Cement Opacifier (2003), cited by 1
- K991893: Parallax Tracer Radiopaque Particles (1999), cited by 1

## Recent decisions
- K033230: Tracers TA Bone Cement Opacifier, Model TCR-TA (Dec 12, 2003)
- K023445: Tracers Bone Cement Opacifier (Mar 11, 2003)
- K022169: Clearview Plus Bone and Vertebral Body Biopsy Needles (Jul 25, 2002)
- K011206: Parallax Bone and Vertebral Body Biopsy and Infusion Needles (Jul 18, 2001)
- K994022: Parallax Cranioset (Aug 31, 2000)
- K991893: Parallax Tracer Radiopaque Particles (Aug 13, 1999)

Source page: https://510kreport.com/company/parallax-medical