# Gynetech Pty., Ltd.

- Location (FDA's records): Richmond, AU
- FDA decisions: 5 (1995–2015): 5 510(k) clearances
- Names in FDA's records: Gynetech Pty. , Ltd. (4); Gynetech, Inc. (1)
- Product codes: LKF (2), HHT (1), HIF (1), HEW (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (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
- Genicon, LC: 1 (https://510kreport.com/company/genicon-lc)
- Conmed Corporation: 1 (https://510kreport.com/company/conmed)
- CooperSurgical, Inc.: 1 (https://510kreport.com/company/coopersurgical)

## Firms that cite its devices most
- Applied Medical Resources: 1 (https://510kreport.com/company/applied-medical-resources)

## Its most-cited devices
- K142164: Manipulator; Manipulator Pro (2014), cited by 1
- K051594: Mccartney Access Tube (2005), cited by 1

## Recent decisions
- K150519: ManipulatOR PRO, ManipulatOR (Aug 19, 2015)
- K142700: InsufflatOR Needle (Dec 19, 2014)
- K142164: Manipulator; Manipulator Pro (Dec 17, 2014)
- K051594: Mccartney Access Tube (Sep 2, 2005)
- K954562: Gynetech P.O.S. Spap Smear Cell Collection & Transport Kit (Dec 22, 1995)

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