# Ximed/Prosure/Injectx

- Location (FDA's records): San Jose, CA
- FDA decisions: 9 (1995–2001): 9 510(k) clearances
- Product codes: GEI (4), GAA (2), FAS (2), FBK (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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 that cite its devices most
- Wilson-Cook Medical, Inc.: 1 (https://510kreport.com/company/wilson-cook-medical)
- Arvik Enterprises/ Mini Lap Technologies: 1 (https://510kreport.com/company/arvik-enterprises-mini-lap-technologies)
- Cook Endoscopy: 1 (https://510kreport.com/company/cook-endoscopy)
- Cook Urological, Inc.: 1 (https://510kreport.com/company/cook-urological)

## Its most-cited devices
- K994151: Percutx-Injection/Aspiration Needle Probes/Devices (2000), cited by 2
- K983200: Injection/Aspiration Needles Probes/Devices-Tpi/Tpi Flex (1998), cited by 1
- K983765: Injection Needle Probe/Device-Tunis (1998), cited by 1

## Recent decisions
- K002269: Electrosurgical Probes and Devices-Geltx (Jan 4, 2001)
- K994151: Percutx-Injection/Aspiration Needle Probes/Devices (Mar 1, 2000)
- K983200: Injection/Aspiration Needles Probes/Devices-Tpi/Tpi Flex (Dec 11, 1998)
- K983765: Injection Needle Probe/Device-Tunis (Dec 11, 1998)
- K981256: Isolated Saline Electrodes/Probes/Devices-Salinetrode (May 12, 1998)
- K974484: Isolated Electrosurgical Probes and Devices-Salinetrode (Feb 10, 1998)
- K974637: Electrodes/Probes/Devices (Jan 7, 1998)
- K962593: Electrosurgical Probes & Devices (Nov 12, 1996)

Source page: https://510kreport.com/company/ximed-prosure-injectx
