A2 Medical Systems, LLC
United StatesFDA 510(k) applicant, unverified FDA FEI 3020965506
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
angiOCCLUDE Ligating Clips Ref K230966
510(k) 510(k)angioLOCK Polymer Ligating Clip Ref K220006
510(k) 510(k)
Company details
- FDA FEI number
- 3020965506
- Address
- 6387 Technology Avenue, Kalamazoo, MI, 49009
Frequently asked questions
How many devices does A2 Medical Systems, LLC have in the registry?
The registry currently lists 2 devices for A2 Medical Systems, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list A2 Medical Systems, LLC's devices?
Among its 2 most recently registered devices, A2 Medical Systems, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do A2 Medical Systems, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for A2 Medical Systems, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A2 Medical Systems, LLC in the registry?
The most recently registered devices listed for A2 Medical Systems, LLC include angiOCCLUDE Ligating Clips and angioLOCK Polymer Ligating Clip.