L. Keroack Co.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What L. Keroack Co. makes
L. Keroack Co. manufactures the DENSICOMP 250, a medical device designed for measuring and analyzing bone mineral density, commonly used in diagnostic imaging for osteoporosis assessment.
The company’s portfolio is regulated under Class II devices in the US, with the DENSICOMP 250 authorised via the FDA’s 510(k) clearance process. The device is listed in the FDA’s 510(k) registry.
Catalogue
Densicomp 250 Ref K904587
510(k) 510(k)
Frequently asked questions
How many devices does L. Keroack Co. have in the registry?
The registry currently lists 1 device for L. Keroack Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list L. Keroack Co.'s devices?
Among its 1 most recently registered device, L. Keroack Co. has devices listed in FDA 510(k) (1 device).
What risk classes do L. Keroack Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for L. Keroack Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from L. Keroack Co. in the registry?
The most recently registered devices listed for L. Keroack Co. include DENSICOMP 250.