# Vascumetrix, LLC

- Location (FDA's records): Mesa, AZ
- FDA decisions: 3 (2001–2003): 3 510(k) clearances
- Product codes: DRE (3)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 2 (2 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
- Endovascular Instruments, Inc.: 1 (https://510kreport.com/company/endovascular-instruments)

## Its most-cited devices
- K012256: Gelbish Vascular Dilator (2001), cited by 2

## Recent decisions
- K030260: Gelbfish Flex Vascular Dilator (Feb 20, 2003)
- K023507: Modification to Gelbfish Vascular Dilators (Nov 8, 2002)
- K012256: Gelbish Vascular Dilator (Dec 20, 2001)

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