Dynasthetics

FDA registration: United States Last updated 25 Oct 2026

Catalogue14

Sovant SV1000 Ref SV1000

Class II FDA UDI Active
SmartProngs Cannula 24001 Ref 24001

Class II FDA UDI Active
VeyO2 Mask 24002 Ref 24002

Class II FDA UDI Active
Sovant EMS Instrument SV500 Ref SV500

Class II FDA UDI Active
VeyO2 M Mask Assy, Single 24003 Ref 24003

Class II FDA UDI Active
Sovant Cannula with Microstream Adapter P/N 23008 Ref P/N 23008

Class II FDA UDI Active
Sovant VeyO2 mask with Microstream adapter 23009 Ref 23009

Class II FDA UDI Active
Sovant VeyO2 mask with Microstream adapter 23010 Ref 23010

Class II FDA UDI Active
SmartProngs Cannula 24001 Ref 24001

Class II FDA UDI Active
Sovant SV1000 Ref SV1000

Class II FDA UDI Active
Vapor Clean 10000 Ref 10000

Class II FDA UDI Active
Vapor Clean 10000 Ref 10000

Class II FDA UDI Active
VeyO2 Mask 24002 Ref 24002

Class II FDA UDI Active
Proxima Ref K220591

Class II FDA 510(k) Active

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

2022
- 9 May 2022 Z-1591-2023 Class II Ongoing Due to a manufacturing issue that may result in filter leakage.