Aventamed Dac is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Aventamed Dac - FDA 510(k) Cleared Devices
Recent clearances: 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)), Solo+ Tympanostomy Tube Device (TTD)
2
Total
2
Cleared
0
Denied
Aventamed Dac has 2 FDA 510(k) cleared medical devices. Based in Bishopstown, IE.
Latest FDA clearance: Apr 2025. Active since 2024. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Aventamed Dac Filter by specialty or product code using the sidebar.
2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Aventamed Dac
2 devices