Ladd Research Industries, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Ladd Research Industries, Inc. makes
Ladd Research Industries, Inc. manufactures intracranial pressure (ICP) monitoring devices, including the LADD/STERITEK ICP MONITOR (P3000), the LADD MEDICAL S-2000, and the MINI-MONITOR J7000. These products are designed for clinical use in measuring and displaying ICP in neurosurgical and critical care settings, supporting patient monitoring in high-risk conditions.
The company’s ICP monitors are classified as Class II medical devices under FDA regulations and are listed via 510(k) clearance. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
Ladd/Steritek Icp Monitor, Cat. No. P3000 Ref K862820
Regimes: 510(k) Registry: 510(k)Ladd Medical S-2000 Ref K862012
Regimes: 510(k) Registry: 510(k)Mini-Monitor J7000 Icp Ref K893395
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ladd Research Industries, Inc. have in the registry?
The registry currently lists 3 devices for Ladd Research Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ladd Research Industries, Inc.'s devices?
Among its 3 most recently registered devices, Ladd Research Industries, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ladd Research Industries, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ladd Research Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ladd Research Industries, Inc. in the registry?
The most recently registered devices listed for Ladd Research Industries, Inc. include LADD/STERITEK ICP MONITOR, CAT. NO. P3000, LADD MEDICAL S-2000 and MINI-MONITOR J7000 ICP.