# Aventamed Dac

- Location (FDA's records): Bishopstown, IE
- FDA decisions: 2 (2024–2025): 2 510(k) clearances
- Product codes: ETD (2)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (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
- Preceptis Medical: 2 (https://510kreport.com/company/preceptis-medical)

## Its most-cited devices
- K232702: Solo+ Tympanostomy Tube Device (TTD) (2024), cited by 1

## Recent decisions
- K250256: Solo+ Tympanostomy Tube Device (TTD), Solo+ TTD, Solo+ (Solo+ Tympanostomy Tube Handpiece (Catalogue #: 12115-100-000) and Solo+ Tympanostomy Tube Cartridge (Catalogue #: 12115-200-000)) (Apr 28, 2025)
- K232702: Solo+ Tympanostomy Tube Device (TTD) (May 20, 2024)

Source page: https://510kreport.com/company/aventamed-dac