# Itl Corporation Pty, Ltd.

- Location (FDA's records): Fyshwick, Canberra Act, AU
- FDA decisions: 5 (1999–2016): 5 510(k) clearances
- Product codes: JKA (2), HAM (1), HIB (1), FMI (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 3 (1 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
- Nipro Medical Corporation: 1 (https://510kreport.com/company/nipro-medical)
- Olsen Electrosurgical, Inc.: 1 (https://510kreport.com/company/olsen-electrosurgical)
- Marketing Perspectives: 1 (https://510kreport.com/company/marketing-perspectives)
- Medisystems Corp.: 1 (https://510kreport.com/company/medisystems)

## Firms that cite its devices most
- Nipro Medical Corporation: 1 (https://510kreport.com/company/nipro-medical)
- Medical Action Industries, Inc.: 1 (https://510kreport.com/company/medical-action-industries)

## Its most-cited devices
- K021941: Samplok Luer Kit (2002), cited by 1
- K000777: Samplok (2000), cited by 1
- K021017: Leespec Disposable Vaginal Speculum (2002), cited by 1

## Recent decisions
- K153472: Quiver Laparoscopic Extendable (Jun 23, 2016)
- K021941: Samplok Luer Kit (Jul 2, 2002)
- K021017: Leespec Disposable Vaginal Speculum (Jun 19, 2002)
- K000777: Samplok (Apr 11, 2000)
- K991404: Platypus AV Fistula Needle Protector (Avfnp) (May 14, 1999)

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