Pan Medical, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 3
What Pan Medical, Ltd. makes
Pan Medical, Ltd. manufactures a range of kyphoplasty catheters designed for vertebral augmentation procedures. These include standard InterV Kyphoplasty Catheters in balloon lengths of 10, 15, and 20mm, as well as miniaturised versions such as the Mini, Micro, and Mini-Flex models (11G and 13G). The catheters are intended for use in percutaneous balloon kyphoplasty to treat vertebral compression fractures.
The company’s kyphoplasty catheters are classified as Class II medical devices under US regulations and are listed in the FDA’s 510(k) registry. These devices are intended for commercial distribution within the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pan Medical, Ltd. have in the registry?
The registry currently lists 3 devices for Pan Medical, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pan Medical, Ltd.'s devices?
Among its 3 most recently registered devices, Pan Medical, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Pan Medical, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Pan Medical, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pan Medical, Ltd. in the registry?
The most recently registered devices listed for Pan Medical, Ltd. include INTER V KYPHOPLASTY CATHETER (BALLOON LENGTH: 0 MM), INTERV KYPHOPLASTY CATHETER (BALLOON LENGHT: 15 MM), INTERV KYPHOPL, InterV Kyphoplasty Catheter (Balloon Length: 10, 15 and 20mm) InterV Kyphoplasty Catheter (Mini) (Balloon Length: 10, 15 and 20mm) and 13G InterV Kyphoplasty Catheter (Micro) and 11G InterV Kyphoplasty Catheter (Mini-Flex).