# Control Medical Technology

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 4 (2012–2020): 4 510(k) clearances
- Names in FDA's records: Control Medical Technology (2); Control Medical Technology, LLC (2)
- Product codes: QEZ (3), FMF (1)
- Predicates its devices cite: 12 (3 its own); citations of its devices by later devices: 5 (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
- Vascular Solutions, Inc.: 3 (https://510kreport.com/company/vascular-solutions)
- Medtronic Vascular: 2 (https://510kreport.com/company/medtronic-vascular)
- Lumen Biomedical, Inc.: 2 (https://510kreport.com/company/lumen-biomedical)
- Pinyons Medical Technology, Inc.: 1 (https://510kreport.com/company/pinyons-medical-technology)
- Kaneka Pharma America, LLC: 1 (https://510kreport.com/company/kaneka-pharma-america)

## Firms that cite its devices most
- 2mg, Inc.: 1 (https://510kreport.com/company/2mg)
- Control Medical Technology, Inc. / Dba Ventiv Scientific: 1 (https://510kreport.com/company/control-medical-technology-dba-ventiv-scientific)

## Its most-cited devices
- K113757: Aspire Max Aspiration Catheter (2012), cited by 3
- K200871: Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical Aspirator (2020), cited by 1
- K131998: Aspire RX-LP6 Aspiration Catheter (2013), cited by 1

## Recent decisions
- K200629: Aspire Mechanical Aspirator G (May 29, 2020)
- K200871: Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical Aspirator (May 4, 2020)
- K131998: Aspire RX-LP6 Aspiration Catheter (Nov 26, 2013)
- K113757: Aspire Max Aspiration Catheter (Feb 22, 2012)

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