Vismed, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Vismed, Inc. makes
Vismed, Inc. manufactures the LD 400, a device for low-dose radiation therapy, and the TKS 4000 AUTO PERIMETER, an automated perimeter measurement tool for ophthalmic use.
The company’s portfolio is regulated under Class I medical devices in the US, with devices listed via the FDA’s 510(k) pathway. Vismed, Inc. is based in the United States.
Catalogue
Ld 400 Ref K930937
Regimes: 510(k) Registry: 510(k)Tks 4000 Auto Perimeter Ref K873122
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vismed, Inc. have in the registry?
The registry currently lists 2 devices for Vismed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vismed, Inc.'s devices?
Among its 2 most recently registered devices, Vismed, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Vismed, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Vismed, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Vismed, Inc. in the registry?
The most recently registered devices listed for Vismed, Inc. include LD 400 and TKS 4000 AUTO PERIMETER.