# Biomedix, Inc.

- Location (FDA's records): Spencer, IN
- FDA decisions: 11 (1993–2014): 11 510(k) clearances
- Product codes: JOM (3), FPA (3), CGA (2), JAF (2), BTR (1)
- Predicates its devices cite: 9 (6 its own); citations of its devices by later devices: 10 (6 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Lifescan, Inc.: 2 (https://510kreport.com/company/lifescan)
- Polymer Technology Systems, Inc.: 1 (https://510kreport.com/company/polymer-technology-systems)

## Firms that cite its devices most
- Padtest, LLC: 1 (https://510kreport.com/company/padtest)
- Collaborative Care Diagnostics, LLC, D.B.A. Biomedix: 1 (https://510kreport.com/company/collaborative-care-diagnostics-dba-biomedix)
- Atys Medical: 1 (https://510kreport.com/company/atys-medical)
- Summit Doppler Systems, Inc.: 1 (https://510kreport.com/company/summit-doppler-systems)

## Its most-cited devices
- K042616: Biomedix Padnet Lab (2004), cited by 3
- K973644: Flostat Vascular Lab (1997), cited by 3
- K122281: Padnet 2.0 (2012), cited by 1
- K073146: Padnet+ (2007), cited by 1
- K925645: SELEC-3 (1993), cited by 1
- K033627: Q.Steps Biometer G Blood Glucose Monitoring System (2004), cited by 1

## Recent decisions
- K142097: Selec-3 I.V.Administration Set (Aug 29, 2014)
- K122281: Padnet 2.0 (Aug 29, 2012)
- K073146: Padnet+ (Nov 21, 2007)
- K050182: Q.Steps Biometer G/C Dual Monitoring System (Aug 9, 2005)
- K042616: Biomedix Padnet Lab (Oct 12, 2004)
- K033627: Q.Steps Biometer G Blood Glucose Monitoring System (May 21, 2004)
- K973857: Flostat Vascular Report Generator (VRG) (Dec 29, 1997)
- K973644: Flostat Vascular Lab (Dec 23, 1997)

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