Vertex Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 21
What Vertex Medical Corp. makes
Vertex Medical Corp. manufactures medical devices for vascular access, monitoring, and drainage, including polyethylene monitoring connectors, dilation catheters, and angiographic syringes. Their portfolio includes reusable needles, percutaneous catheter introducer sets, nephrostomy/biliary drainage bags, and protective sleeves for procedural use. The company also produces monitoring catheters and vessel dilators designed for interventional radiology and cardiovascular applications.
The company’s devices are regulated under FDA 510(k) clearance, with products classified as Class II and Unclassified (U). These devices are listed in the FDA’s 510(k) registry, adhering to U.S. medical device regulations. Vertex Medical Corp. is based in the United States.
Catalogue
Search and filter all 21 devicesFrequently asked questions
How many devices does Vertex Medical Corp. have in the registry?
The registry currently lists 21 devices for Vertex Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vertex Medical Corp.'s devices?
Among its 21 most recently registered devices, Vertex Medical Corp. has devices listed in FDA 510(k) (21 devices).
What risk classes do Vertex Medical Corp.'s devices fall under?
Among its 21 most recently registered devices, the classes recorded for Vertex Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vertex Medical Corp. in the registry?
The most recently registered devices listed for Vertex Medical Corp. include BACKSTOP VALVE W/SIDE ARM, POLYETHYLENE MONITORING CONNECTORS, VERTEX MONITORING CATHETER and ULTRA-ASEPT ANGIOGRAPHIC SYRINGE/SPARE.