Menlo Care, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 31
What Menlo Care, Inc. makes
Menlo Care, Inc. manufactures vascular access devices, including single-lumen, multilumen, and midline catheters for peripheral and central venous access, such as the VERSACATH SELECTALUMEN INNER CATHETER and LANDMARK DUAL-LUMEN MIDLINE CATHETER SYSTEM. Their portfolio also includes urinary diversion stents, such as the MENLO CARE URINARY DIVERSION STENT, and specialized catheter placement units like the STREAM LINE I.V. CATHETER PLACEMENT UNIT. Additional products include PICC line systems like the SAFE-PICC CATHETER and INTROPEEL V, as well as catheter trays and add-a-lumen kits for extended vascular access.
Menlo Care’s devices are classified under FDA categories including Class I, Class II, and Unclassified (U), with many listed via the 510(k) pathway. The company’s products are registered with the FDA’s 510(k) clearance process, and the manufacturer is based in the United States.
Catalogue
Search and filter all 31 devicesFrequently asked questions
How many devices does Menlo Care, Inc. have in the registry?
The registry currently lists 31 devices for Menlo Care, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Menlo Care, Inc.'s devices?
Among its 31 most recently registered devices, Menlo Care, Inc. has devices listed in FDA 510(k) (31 devices).
What risk classes do Menlo Care, Inc.'s devices fall under?
Among its 31 most recently registered devices, the classes recorded for Menlo Care, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Menlo Care, Inc. in the registry?
The most recently registered devices listed for Menlo Care, Inc. include VERSACATH SELECTALUMEN INNER CATHETER, INTROPEEL V, SAFE-PICC CATHETER and STREAMLINE VASCULAR ACCESS DEVICE.