Amsino Medical Inc.
United Statesfrom the FDA registration address FDA establishment FEI 3016248619
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
AMSure® Single Use Saline Topical Solution Ref K201138
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3016248619
- Address
- 700 Enterprise St., Aurora, IL, 60504
Frequently asked questions
How many devices does AMSINO MEDICAL INC. have in the registry?
The registry currently lists 1 device for AMSINO MEDICAL INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list AMSINO MEDICAL INC.'s devices?
Among its 1 most recently registered device, AMSINO MEDICAL INC. has devices listed in FDA 510(k) (1 device).
What are the newest devices from AMSINO MEDICAL INC. in the registry?
The most recently registered devices listed for AMSINO MEDICAL INC. include AMSure® Single Use Saline Topical Solution.