Luconex, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Luconex, Inc. makes
Luconex, Inc. manufactures mobile and fixed standing devices designed for patient care, including the B.A.C. 3000 chair/stander and the B.A.C. 1000 mobile standing device. These products are intended to assist patients in achieving an upright position for mobility, therapy, or comfort.
The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
B.A.C. 3000 Chair/Stander Ref K896904
Regimes: 510(k) Registry: 510(k)B.A.C. 1000 Mobile Standing Device Ref K884840
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Luconex, Inc. have in the registry?
The registry currently lists 2 devices for Luconex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Luconex, Inc.'s devices?
Among its 2 most recently registered devices, Luconex, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Luconex, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Luconex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Luconex, Inc. in the registry?
The most recently registered devices listed for Luconex, Inc. include B.A.C. 3000 CHAIR/STANDER and B.A.C. 1000 MOBILE STANDING DEVICE.