Limestone Technologies, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Limestone Technologies, Inc. makes
Limestone Technologies, Inc. develops the PrefTest Professional Suite, a software tool designed for pre-implant planning and patient-specific simulation in orthopedic procedures, particularly for joint replacements.
The company’s portfolio is regulated under FDA Class II (U) devices and is listed in the FDA 510(k) database. The manufacturer is based in the United States.
Catalogue
Preftest Professional Suite Ref K052929
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Limestone Technologies, Inc. have in the registry?
The registry currently lists 1 device for Limestone Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Limestone Technologies, Inc.'s devices?
Among its 1 most recently registered device, Limestone Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Limestone Technologies, Inc. in the registry?
The most recently registered devices listed for Limestone Technologies, Inc. include PREFTEST PROFESSIONAL SUITE.