A&A Ent.
Country not established
- Devices
- 2
What A&A Ent. makes
A&A Ent. manufactures coronary artery bypass graft (CABG) rings, which are used in surgical procedures to support arterial grafts, and vein clamps, which assist in isolating and securing veins during vascular surgery.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Cabg Rings Ref K771819
510(k) 510(k)Vein Clamps Ref K772137
510(k) 510(k)
Frequently asked questions
How many devices does A&A Ent. have in the registry?
The registry currently lists 2 devices for A&A Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list A&A Ent.'s devices?
Among its 2 most recently registered devices, A&A Ent. has devices listed in FDA 510(k) (2 devices).
What risk classes do A&A Ent.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for A&A Ent.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A&A Ent. in the registry?
The most recently registered devices listed for A&A Ent. include CABG RINGS and VEIN CLAMPS.