A-1 Engineering
Country not established FDA FEI 3008069988
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What A-1 Engineering makes
A-1 Engineering manufactures the Body System and the NeurotriS series, specifically the SX2500 and SX3800 models.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Body System Ref K182440
510(k) 510(k)NeurotriS (SX2500); NeurotriS (SX3800) Ref K251909
510(k) 510(k)
Company details
- FDA FEI number
- 3008069988
- Address
- 30 Mauchly Ste A, Irvine, CA, 92618
Frequently asked questions
How many devices does A-1 Engineering have in the registry?
The registry currently lists 2 devices for A-1 Engineering. Devices recorded under merged duplicate company entries are counted once.
Which registries list A-1 Engineering's devices?
Among its 2 most recently registered devices, A-1 Engineering has devices listed in FDA 510(k) (2 devices).
What risk classes do A-1 Engineering's devices fall under?
Among its 2 most recently registered devices, the classes recorded for A-1 Engineering's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A-1 Engineering in the registry?
The most recently registered devices listed for A-1 Engineering include Body System and NeurotriS (SX2500); NeurotriS (SX3800).