Lexicor Medical Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Lexicor Medical Technology, Inc. makes
Lexicor Medical Technology, Inc. manufactures the NeuroSearch-24 (NRS-24) and the MRS-2D, which are medical devices designed for neurological monitoring and recording purposes.
These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Neurosearch-24 Or Nrs-24 Ref K904269
Regimes: 510(k) Registry: 510(k)Neurosearch-24 Or Nrs-24 Ref K915820
Regimes: 510(k) Registry: 510(k)Neba System Ref DEN110019
Regimes: De Novo Registry: De NovoMrs-2D Ref K961645
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lexicor Medical Technology, Inc. have in the registry?
The registry currently lists 4 devices for Lexicor Medical Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lexicor Medical Technology, Inc.'s devices?
Among its 4 most recently registered devices, Lexicor Medical Technology, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Lexicor Medical Technology, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Lexicor Medical Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lexicor Medical Technology, Inc. in the registry?
The most recently registered devices listed for Lexicor Medical Technology, Inc. include NEUROSEARCH-24 OR NRS-24, NEBA SYSTEM and MRS-2D.