# Oventus Manufacturing Pty, Ltd.

- Location (FDA's records): Indooroopilly, AU
- FDA decisions: 4 (2016–2019): 4 510(k) clearances
- Product codes: LRK (4)
- 510(k) review time since 2016: median 74 days, against 157 for FDA's reviews in the same codes and years (3 of 4 faster)
- Predicates its devices cite: 8 (4 its own); citations of its devices by later devices: 6 (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
- Airway Management, Inc.: 2 (https://510kreport.com/company/airway-management)
- Dyna Flex: 1 (https://510kreport.com/company/dyna-flex)
- Somnomed, Inc.: 1 (https://510kreport.com/company/somnomed)

## Firms that cite its devices most
- Meris Investment Group: 1 (https://510kreport.com/company/meris-investment-group)
- Greystone Ip, Ltd.: 1 (https://510kreport.com/company/greystone-ip)

## Its most-cited devices
- K160234: OVENT (2016), cited by 2
- K190236: O2Vent Optima (2019), cited by 2
- K161832: O2VENT T (2016), cited by 1
- K171316: O2Vent W (2017), cited by 1

## Recent decisions
- K190236: O2Vent Optima (Aug 29, 2019)
- K171316: O2Vent W (Jul 11, 2017)
- K161832: O2VENT T (Sep 23, 2016)
- K160234: OVENT (Mar 17, 2016)

Source page: https://510kreport.com/company/oventus-manufacturing