Highpoint Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Highpoint Medical Corp. makes
Highpoint Medical Corp. manufactures medical devices designed to address intraoperative challenges in ophthalmic surgery, including a catheter control system and a lens fog reduction device to minimize fogging during procedures.
The company’s portfolio is classified under FDA’s Class II devices and is listed in the 510(k) registry, reflecting regulatory compliance with U.S. medical device authorisation requirements. The manufacturer operates from the United States.
Catalogue
Cath Control Ref K914211
Regimes: 510(k) Registry: 510(k)Fog Control, Lens Fog Reduction Device Ref K932300
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Highpoint Medical Corp. have in the registry?
The registry currently lists 2 devices for Highpoint Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Highpoint Medical Corp.'s devices?
Among its 2 most recently registered devices, Highpoint Medical Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Highpoint Medical Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Highpoint Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Highpoint Medical Corp. in the registry?
The most recently registered devices listed for Highpoint Medical Corp. include CATH CONTROL and FOG CONTROL, LENS FOG REDUCTION DEVICE.