Sandstrom Trade & Technology, Inc.
CanadaFDA applicant, unverified
- Devices
- 2
What Sandstrom Trade & Technology, Inc. makes
Sandstrom Trade & Technology, Inc. manufactures stereotactic surgical systems, including the Laiteten Stereotactic System and Laiteten’s Trigeminus Stereoguide, designed for precise brain and cranial procedures.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
The Laitinen Stereotactic System Ref K881131
Regimes: 510(k) Registry: 510(k)Laitinen's Trigeminus Stereoguide Ref K881132
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sandstrom Trade & Technology, Inc. have in the registry?
The registry currently lists 2 devices for Sandstrom Trade & Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sandstrom Trade & Technology, Inc.'s devices?
Among its 2 most recently registered devices, Sandstrom Trade & Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Sandstrom Trade & Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sandstrom Trade & Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sandstrom Trade & Technology, Inc. in the registry?
The most recently registered devices listed for Sandstrom Trade & Technology, Inc. include THE LAITINEN STEREOTACTIC SYSTEM and LAITINEN'S TRIGEMINUS STEREOGUIDE.