# Flexicath, Ltd.

- Location (FDA's records): Tel Aviv, IL
- FDA decisions: 4 (2007–2012): 4 510(k) clearances
- Product codes: FOZ (3), LJS (1)
- Predicates its devices cite: 8 (4 its own); citations of its devices by later devices: 4 (4 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
- Medical Components, Inc.: 1 (https://510kreport.com/company/medical-components)
- Plastimed Laboratoire Pharmaceutique: 1 (https://510kreport.com/company/plastimed-laboratoire-pharmaceutique)
- Teleflexmedical, Inc.: 1 (https://510kreport.com/company/teleflexmedical)
- Arrow Intl., Inc.: 1 (https://510kreport.com/company/arrow-intl)

## Its most-cited devices
- K080793: Firmgrip (2008), cited by 2
- K063363: Firmgrip Peripherally Inserted Catheter Device (2007), cited by 1
- K092629: SNM Firmgrip (2009), cited by 1

## Recent decisions
- K111939: M/29TM - Pressure Injectable (Jul 11, 2012)
- K092629: SNM Firmgrip (Sep 25, 2009)
- K080793: Firmgrip (Oct 16, 2008)
- K063363: Firmgrip Peripherally Inserted Catheter Device (May 7, 2007)

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