Laurus Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Curvilinear Suture Placement System Ref K973415
Regimes: 510(k) Registry: 510(k)Stereotactic Needle Core Biopsy System Ref K973215
Regimes: 510(k) Registry: 510(k)Laurus Needle Core Biopsy System Ref K960317
Regimes: 510(k) Registry: 510(k)Disposable Suture Placement System Ref K932553
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laurus Medical Corp. have in the registry?
The registry currently lists 4 devices for Laurus Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laurus Medical Corp.'s devices?
Among its 4 most recently registered devices, Laurus Medical Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Laurus Medical Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Laurus Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laurus Medical Corp. in the registry?
The most recently registered devices listed for Laurus Medical Corp. include CURVILINEAR SUTURE PLACEMENT SYSTEM, STEREOTACTIC NEEDLE CORE BIOPSY SYSTEM, LAURUS NEEDLE CORE BIOPSY SYSTEM and DISPOSABLE SUTURE PLACEMENT SYSTEM.