# Intelesens Limited

- Location (FDA's records): Bonita Springs, FL
- FDA decisions: 4 (2011–2016): 4 510(k) clearances
- Names in FDA's records: Intelesens Limited (3); Intelesens, Ltd. (1)
- Product codes: MHX (3), DSI (1)
- Predicates its devices cite: 7 (2 its own); citations of its devices by later devices: 3 (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
- Biomedical Systems Corp.: 1 (https://510kreport.com/company/biomedical-systems)
- Datascope Corp.: 1 (https://510kreport.com/company/datascope)
- Proteus Biomedical, Inc.: 1 (https://510kreport.com/company/proteus-biomedical)
- Cadi Scientific Pte.Ltd: 1 (https://510kreport.com/company/cadi-scientific)
- Welch Allyn Protocol, Inc.: 1 (https://510kreport.com/company/welch-allyn-protocol)

## Firms that cite its devices most
- Lifewatch Technologies, Ltd.: 1 (https://510kreport.com/company/lifewatch-technologies)

## Its most-cited devices
- K110015: Vitalsens, Aingeal, V-Pod (2011), cited by 3

## Recent decisions
- K153275: Aingeal Activity System (Feb 26, 2016)
- K151027: zensor system (Oct 2, 2015)
- K131000: V-Patch System (Jan 8, 2014)
- K110015: Vitalsens, Aingeal, V-Pod (May 20, 2011)

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