The LE Blanc Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What The LE Blanc Corp. makes
The LE Blanc Corp. manufactures the ASTRO TRACE systems, including the Model AT-01 and Model AT-02, which are designed for medical imaging applications.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Astro Trace (Model At-01) Ref K884592
Regimes: 510(k) Registry: 510(k)Astro Trace (Model At-02) Ref K885137
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The LE Blanc Corp. have in the registry?
The registry currently lists 2 devices for The LE Blanc Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The LE Blanc Corp.'s devices?
Among its 2 most recently registered devices, The LE Blanc Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do The LE Blanc Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for The LE Blanc Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The LE Blanc Corp. in the registry?
The most recently registered devices listed for The LE Blanc Corp. include ASTRO TRACE (MODEL AT-01) and ASTRO TRACE (MODEL AT-02).