# Medevice, Inc.

- Location (FDA's records): Canada L4w 4m2, CA
- FDA decisions: 6 (1989–2009): 6 510(k) clearances
- Names in FDA's records: Medevice, Inc. (5); Medevice Corporation (1)
- Product codes: BSO (2), KNT (1), BWK (1), FPA (1), FOZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (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
- PAJUNK GmbH Medizintechnologie: 1 (https://510kreport.com/company/pajunk-medizintechnologie)

## Its most-cited devices
- K901129: Bio-Mate (TM) Pediatric Epidural Catheter (1990), cited by 1

## Recent decisions
- K091875: E-Pulse (Dec 7, 2009)
- K072550: Sightsure Operational Indicator, Model SS301 (Dec 7, 2007)
- K920638: Bio-Mate Pic Catheter (Mar 26, 1993)
- K912856: Mede-Flo I.V. Extension Set (Dec 17, 1991)
- K901129: Bio-Mate (TM) Pediatric Epidural Catheter (Mar 30, 1990)
- K884969: Bio-Mate (TM) Epidural Catheter (Jun 23, 1989)

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